10x Genomics Acquires Proteintech Genomics, Expanding Proteomics Capablities

10x Genomics has acquired Proteintech Genomics for an undisclosed price, the companies said, in a deal driven by the buyer’s commitment to expanding its multiomics presence—in this case, by strategically expanding its proteomics capabilities.

The acquisition is intended to bring together 10x’s expertise in scalable single-cell and spatial biology platforms with Proteintech Genomics’ capabilities in protein detection. Founded in 2022, Proteintech Genomics specializes in life science technologies enabling researchers to apply single-cell and spatial multiomics tools toward discovery. The company develops fully optimized and highly multiplexed proteomic assays designed for ready integration into various single-cell and spatial analysis application workflows.

By helping researchers harmonize RNA and protein analysis, Proteintech Genomics has positioned itself as an alternative to the multiple vendors and their workflows traditionally needed to accomplish both analyses, as researchers increasingly combine transcriptomic- and proteomics-based data to gain complementary insights into cellular identity, state, and function.

“Proteintech Genomics strengthens our capabilities in one of the most exciting and rapidly evolving areas of biology: proteomics,” Michael Schnall-Levin, 10x’s CTO, chief strategy officer, and founding scientist, told GEN. “While transcriptomic technologies have advanced tremendously over the last decade, we believe there is still significant opportunity to push protein-based analysis much further, particularly in combination with RNA and other analytes.”

“We believe the future of biological analysis will increasingly integrate single-cell, proteomic, and spatial information,” Schnall-Levin added. “This acquisition reflects our conviction that proteomics will be an important part of that future and expands our ability to support richer multiomic workflows across our portfolio.”

Among Proteintech Genomics’ technologies is its Human Discovery Panel, which, according to the company, is the largest antibody-based single-cell protein panel. The panel allows researchers to simultaneously profile 347 DNA-barcoded antibodies covering 325 distinct protein targets, alongside transcriptomic measurements.

“Significant opportunities”

“We see significant opportunities to continue expanding both plex and content over time. One of the exciting aspects of bringing Proteintech Genomics into 10x is the ability to invest more deeply in future proteomic innovation,” Schnall-Levin explained. “While we aren’t announcing specific products today, directionally we’re interested in enabling higher-plex measurements, broader biological content, and more accessible workflows. Those are all areas where we see substantial opportunity going forward.”

The Human Discovery Panel is also designed to support integrated analysis of intracellular proteins, cell surface proteins, and transcriptomic profiles within sequencing-compatible workflows. The panel is compatible with 10x’s Flex chemistry, including the Flex Apex assay, the company’s fastest-growing single-cell assay.

“Proteintech Genomics brings innovative protein detection technologies, including the Human Discovery Panel, as well as deep expertise in protein biology, antibody panel development, and assay design. Together, we believe we can move faster, pursue more ambitious product development efforts, and make high-quality multiomic workflows more accessible and scalable for researchers,” Schnall-Levin said.

He said one attraction to 10x of combining with Proteintech Genomics was the combination it offered to 10x of technical performance and ecosystem fit: “Proteintech Genomics has been a longtime 10x partner, and its products were purpose-built to work with 10x workflows. Our customers are already using these technologies together today, which gives us a strong foundation to innovate more quickly and bring even more powerful multiomic capabilities to the field.”

Through its acquisition of Proteintech Genomics, 10x aims to achieve its vision of enabling multimodal biological analysis across its single-cell and spatial platforms—including protein capabilities planned for the Atera spatial platform, unveiled during the American Association for Cancer Research (AACR) conference.

Atera can run up to 800 1 cmwhole transcriptome samples (FFPE and fresh frozen) per year, with flexible run configurations, and a greater than 5 cm² imageable area per slide (for greater than 2,000 mm² total tissue per run when using all four slides). The Atera WTA (Whole Transcriptome Analysis) panel targets more than 18,000 genes, with stackable customization of 1,000-gene Atera Select panels available now—and optional stacking of up to three 1,000-gene panels coming in the future.

“We’ve already spoken publicly about future protein capabilities planned for Atera, and this acquisition strengthens our ability to deliver on that vision while continuing to advance integrated approaches across both our single-cell and spatial platforms, Schnall-Levin said.

Higher-plex proteomics challenge

10x’s interest in higher-plex proteomics makes sense since it is the fastest-growing submarket in the $11 billion core proteomic space, set to grow by double digits, according to Leerink Partners. But a Leerink analyst cautioned that the company will find it challenging to grow in the space as it absorbs costs associated with Atera and Flex Apex.

“TXG leveraging itself to higher-plex proteomics is helpful,” Puneet Souda, senior managing director, life science tools and diagnostics, and a senior research analyst with Leerink, wrote in a research note. “We believe the deal accelerates higher-plex proteomics content for Atera, which adds to its long-term value. TXG can also bundle single-cell proteomic kits, which is a small but growing area of single-cell research.”

“Nonetheless, we still expect the digestion of Flex Apex and Atera-driven freezing/impact to weigh on near-term growth, particularly in a challenged academic funding backdrop,” Souda added.

Investors did not appear to share that concern, as 10x shares dipped 0.6% as of 12:21 p.m. ET, to an even $29.00 from $29.18 at Monday’s close. The share fluctuated between $28.93 and $30.87 during Tuesday morning trading.

Ci Chu, senior vice president, AI-enabled discovery for Xaira Therapeutics, said in a statement included within 10x’s announcement that the acquisition reflected the importance of integrating protein biology with single-cell and spatial technologies.

“Biology is bigger than transcriptomics alone,” Chu stated. “Bringing scalable protein measurements into single cell and spatial biology is an important step toward richer, more predictive views of cellular state—and ultimately, virtual cell models that better reflect the complexity of living systems.”

Potential clinical applications

In addition to facilitating expansion in multiomics, the acquisition of Proteintech Genomics could help 10x achieve another longer-term goal, namely, looking beyond its traditional focus on research tools for academic, government, and industry customers, by strengthening its clinical diagnostic offerings.

10x expanded into clinical diagnostics during the J.P. Morgan 44th Annual Healthcare Conference, when the company announced three partnerships with top-tier institutions: Brigham and Women’s Hospital and Dana-Farber Cancer Institute, both in Boston, as well as the New York-based Cancer Research Institute. 10x also committed to building its own CLIA-certified laboratory within about a year, with the goal of enabling clinical deployment of diagnostics that will come up with such collaborations.

Integrating Proteintech Genomics tools into clinical settings will be a longer-term priority since the company’s offerings are for research use only and not intended for diagnostics procedures.

“Protein measurements are highly relevant to many translational research applications, particularly in areas such as immunology, oncology, and neurology. Researchers in academia and biopharma increasingly want to combine protein and RNA measurements to better understand cellular function, therapeutic response, and disease biology,” Schnall-Levin said. “Longer term, we believe single-cell and spatial proteomics are likely to play a meaningful role in diagnostics.”

10x and Proteintech Genomics did not disclose the price or other financial terms of the acquisition, though 10x said it believes the transaction “will not meaningfully impact its near-term financial outlook.”

10x finished the first quarter with a net loss of $13.47 million, less than half its $34.358 million net loss of Q1 2025, on revenue that shrunk 3% year-over-year, to $150.843 million from $154.883 million in the first three months of last year. The company reported $490.285 million in cash and cash equivalents as of March 31, up 3% from $473.966 million as of December 31, 2025.

Proteintech Genomics is a subsidiary of Proteintech Group, a developer of high-plex proteomic solutions for single-cell and spatial applications; both companies are privately held.

San Diego-based Proteintech Genomics’ workforce consists of what Schnall-Levin described as “a small team of eight people,” including CEO Kristopher Nazor, PhD.

“We’re going to keep that team,” Schnall-Levin declared.

Added Nazor: “From day one, Proteintech Genomics was built around the belief that RNA and protein measurements are most powerful when used together.”

“Because our technologies were designed to integrate with 10x workflows, joining the 10x team feels like a natural next chapter,” Nazor continued. “We are excited about the opportunity to accelerate innovation together and expand access to integrated multiomic approaches for researchers around the world.”

The post 10x Genomics Acquires Proteintech Genomics, Expanding Proteomics Capablities appeared first on GEN – Genetic Engineering and Biotechnology News.

STAT+: Pharmalittle: We’re reading about U.S. pressure on European drug prices, longer shortages, and more

Good morning, everyone, and welcome to the middle of the week. Congratulations on making it this far, and remember, there are only a few more days until the weekend arrives. So keep plugging away. After all, what are the alternatives? While you ponder the possibilities, we invite you to join us for a delightful cup of stimulation. Our choice today is maple cinnamon French toast, a pantry favorite. Remember that no prescription is required — so no need to reach for your abacus to calculate a co-pay or rebate. Meanwhile, here is the latest menu of tidbits to help you on your way. Have a wonderful day, and please do stay in touch. …

The number of prescription drug shortages in the U.S. fell by 23% last year, marking the second consecutive year of declines and the lowest level since 2017, according to a new analysis that otherwise found troubling signs about medicines that are in short supply, STAT says. For instance, the average drug shortage lasted 5.3 years, exceeding the 4.3 years seen in 2024 and greatly outpacing the average two-year shortage experienced in 2019. Moreover, nearly two-thirds of out-of-stock medicines were in short supply for more than three years, and 39% were unavailable for more than five years. Meanwhile, the 75 drugs that were in short supply last year spanned 130 therapeutic categories, indicating that shortages affected a wide range of diseases and patient populations.

In Europe, two divergent paths are emerging as countries grapple with what to do about drug prices, affecting pharma companies and patients across the continent — and testing the influence of the U.S., STAT explains. In the U.K., after a pressure campaign from both pharma companies and the Trump administration, the government has adopted more industry-friendly policies while also simply promising to spend more on medicines. Germany, another of the continent’s biggest markets, is headed in the opposite direction. Facing growing deficits in its health budget, the government has proposed moves that would cut spending and increase the fees the industry has to pay.

Continue to STAT+ to read the full story…

<![CDATA[Explore the brain’s 5 monoamines—beyond serotonin and dopamine—revealing histamine, melatonin, and trace amines shaping sleep, appetite, and mood.]]>

The State of Biologics Testing 2026

The State of Biologics Testing 2026

The success of modern biologics depends not only on groundbreaking science but on the robustness, speed, and credibility of the testing programs that support them. Across the industry, long established testing paradigms are being re-examined as new modalities emerge, regulatory agencies promote innovation and animal reduction, and development timelines continue to compress.

Charles River publishes The State of Biologics Testing 2026 to help document and interpret this moment of change. Based on Charles River’s deep involvement in biologics testing worldwide, and informed by interviews with leaders across biopharma, quality, and regulatory functions, the report captures how organizations are navigating the transition—from traditional compendial methods to advanced technologies, digital tools, and risk-based approaches.

This report is intended to inform discussion and decision making, not to prescribe solutions. Produced in collaboration with GEN, it reflects the collective voice of an industry adapting to new scientific and regulatory realities.

The post The State of Biologics Testing 2026 appeared first on GEN – Genetic Engineering and Biotechnology News.

The Download: the “steroid olympics” and a safer Mythos

This is today’s edition of The Download, our weekday newsletter that provides a daily dose of what’s going on in the world of technology.

The “steroid olympics” were a circus—and a window into our culture

—Amit Katwala

A couple of weeks ago, at a $50 million arena built in a casino parking lot in Las Vegas, I witnessed a libertarian thought experiment come to life. The inaugural Enhanced Games were the first sporting competition where participants were encouraged to take performance-enhancing drugs.

For supporters of the event, the Enhanced Games offered a glimpse of a future in which medical advances push the human race to new heights—and they never have to get old. As I watched the games unfold, two questions bounced around my head: were they right? And what does that mean for the rest of us?

Read the full story to understand the answers.

MIT Technology Review Narrated: a reality check on the AI jobs hysteria

Despite the growing hysteria over AI’s threat to white-collar jobs, there’s still scant evidence that the technology has had a large-scale impact on the labor market.

Analysis of US labor data shows that unemployment in occupations most exposed to AI is actually lower than in less-exposed jobs. There are also no signs that large numbers of workers are shifting from AI-threatened professions into supposedly safer manual-labor jobs.

It’s true that things aren’t great in the job market. But the reason isn’t simply the rise of AI.


—David Rotman

This is our latest story to be turned into an MIT Technology Review Narrated podcast, which we publish each week on Spotify and Apple Podcasts. Just navigate to MIT Technology Review Narrated on either platform, and follow us to get all our new content as it’s released.

The must-reads

I’ve combed the internet to find you today’s most fun/important/scary/fascinating stories about technology.

1 Anthropic has released a “safe” version of Mythos
It promises it has enough guardrails and user limitations to be safe. (BBC)
+ It has a price tag twice as high as the previous flagship system. (NYT $)
+ Anthropic previously claimed Mythos was too dangerous to release. (CNBC)
+ But critics suspect that was a marketing play. (Guardian)
+ Selective access has become a key strategy for AI labs. (Axios)

2 Seattle has banned new data centers for a year
It’s the largest US city to have passed such a moratorium.(Guardian)
+ Its biggest tech firm, Amazon, has tried to stop the ban. (The Verge)
+ The movement to stop data centers is growing. (NYT $)

3 Democratic senators are pushing for a military AI restriction law
They want a human commander to have the final say. (Gizmodo)
+ But humans in the loop in an AI war is an illusion. (MIT Technology Review)

4 SpaceX plans to launch space data center tests by late 2027
Orbital compute is central to the company’s growth pitch. (Reuters $)
+ It’s also shared new designs for its space data centers. (BI)
+ We’d need these four things to put them in orbit. (MIT Technology Review)

5 China has been accused of escalating AI espionage
A report claims Beijing is hacking tech firms to catch up with the US. (CNBC)
+ There are no winners in a US-China AI arms race. (MIT Technology Review)

6 The Trump family has made about $2.3 billion from crypto
While investors lost about the same amount. (Gizmodo)
+ The Trumps risked next-to-nothing on their crypto ventures. (Reuters $)

7 Apple isn’t launching Siri AI in the European Union
It’s blaming EU interoperability requirements. (The Verge)
+Brussels says Apple didn’t try to find a compliance solution. (Reuters $) 

8 China’s new drone rules have spooked its thriving industry 
Drone firms face new commercial barriers. (Financial Times $)
+ China’s drone sector leads the world. (NYT $)

9 A judge has cancelled a trial after finding both legal teams used AI
The case descended into GenAI tools arguing against each other. (404 Media)
+ Courts have been flooded with AI-generated lawsuits. (MIT Technology Review)

10 The dinosaur-killing asteroid created a thriving new ecosystem
Microscopic life flourished in the extended heat. (New Scientist $)

Quote of the day

“AI technologies today are designed by and for WEIRD societies—Western, educated, industrialized, rich, and democratic.” 

—Aditya Vashistha, an assistant professor at Cornell University, tells Rest of World why AI systems don’t serve global needs.

One More Thing

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LAUREN SIMKIN BERKE


Why the definition of design might need a change

The word “design” once carried a far wider set of meanings than it does today. They ranged from the literal and material (like tracing) through the tactical (to contrive and achieve a goal) to the organizational and institutional—the “designation” of people and objects.

Over centuries, as designing became increasingly separated from making, that broader understanding faded. But now there is a growing case for reclaiming the word’s original sense: not just the search for a more beautiful shape, but the shaping of a more beautiful and sustainable world. 

Find out why we should retool the word “design.”

—Nicholas de Monchaux

We can still have nice things

A place for comfort, fun, and distraction to brighten up your day. (Got any ideas? Drop me a line.)

+ This history of humanity’s search for alien life is fascinating.
+ Watch a damaged painting slowly return to life in this art restoration video.
+ Admire young stars across every stage of cosmic formation in this stunning space picture of the month.
+ Daredevil divers have captured the first-ever underwater footage of an adult great white in the Mediterranean Sea.

Deep and repetitive transcranial magnetic stimulation improves motor dysfunction after basal ganglia infarction: preliminary findings on efficacy and electrophysiological mechanisms

ObjectiveTo observe the therapeutic effects of deep transcranial magnetic stimulation (dTMS) and repetitive transcranial magnetic stimulation (rTMS) on upper and lower limb motor dysfunction in patients with basal ganglia infarction, and to preliminarily explore their underlying electrophysiological mechanisms.MethodsThirty patients with motor dysfunction secondary to basal ganglia infarction, hospitalized at the Affiliated Hospital of North Sichuan Medical College between October 2024 and December 2025, were enrolled in this study. All eligible participants were randomly assigned to one of three treatment groups: dTMS (n = 10), rTMS (n = 10), or sham stimulation (n = 10). All patients in the three groups received routine medical treatment and conventional rehabilitation training. On this basis, the dTMS group was treated with 10 Hz dTMS, the rTMS group with 10 Hz rTMS, and the sham stimulation group with sham stimulation, 5 sessions per week for 2 consecutive weeks. Before treatment, on the first day after treatment, and at 30 days after treatment, the Fugl-Meyer Assessment (FMA), Berg Balance Scale (BBS), and Modified Barthel Index (MBI) were used to evaluate motor function of the affected side and activities of daily living. The resting motor threshold (rMT) and central motor conduction time (CMCT) of the affected hemisphere were measured simultaneously.ResultsThe baseline data among the three groups were comparable (all p > 0.05); After treatment, there was a statistically significant interaction between group and time in FMA-UE, FMA-LE, MBI, and BBS scores among the three groups (all p < 0.05); Compared with baseline, FMA-UE, FMA-LE, MBI, and BBS scores were significantly increased on the first day and at 30 days after treatment in all three groups (all p < 0.001); Compared with the sham stimulation group, the dTMS group exhibited higher FMA-UE, FMA-LE, MBI, and BBS scores on the first day and at 30 days after treatment (all p < 0.05); Compared with the rTMS group, the dTMS group showed no significant differences in FMA-UE and MBI scores on the first day after treatment (all p > 0.05), but higher FMA-LE and BBS scores (all p < 0.05), at 30 days after treatment, FMA-UE, FMA-LE, MBI, and BBS scores were all higher in the dTMS group (all p < 0.05). There was a statistically significant interaction between group and time in rMT and upper limb CMCT among the three groups after treatment (all p < 0.05); Compared with baseline, rMT and upper limb CMCT were significantly decreased on the first day and at 30 days after treatment in all three groups (all p < 0.001); Compared with the sham stimulation group, the dTMS group had lower rMT and upper limb CMCT on the first day and at 30 days after treatment (all p < 0.05); Compared with the rTMS group, the dTMS group showed lower rMT and upper limb CMCT on the first day after treatment (p < 0.05), at 30 days after treatment, rMT was lower (p < 0.05), while no significant difference was found in upper limb CMCT (p > 0.05).Conclusion(1) Both high-frequency dTMS and rTMS can improve upper limb motor dysfunction after basal ganglia cerebral infarction to some extent, and the therapeutic effect of dTMS lasts longer; (2) dTMS has a certain rehabilitative effect on lower limb motor and balance function; (3) The mechanisms underlying the improvement of motor dysfunction after basal ganglia cerebral infarction by high-frequency dTMS and rTMS may be associated with increased excitability of the affected cerebral cortex, enhanced function of the corticospinal tract pathway. In addition, dTMS can directly act on deeper and wider brain regions; (4) Both high-frequency dTMS and rTMS are safe.

Acupuncture modulates the microbiota-gut-brain axis to treat irritable bowel syndrome: a mechanistic exploration

Irritable bowel syndrome (IBS) is a common functional gastrointestinal disorder involving dysregulation of the microbiota-gut-brain (MGB) axis. Acupuncture effectively alleviates IBS symptoms, yet its underlying mechanisms remain incompletely understood. This review synthesizes current evidence to propose a mechanistic framework by which acupuncture treats IBS through MGB axis modulation. We systematically examine: (1) MGB axis dysfunction in IBS pathophysiology across neural, endocrine, and immune pathways; (2) acupuncture’s modulation of gut microbiota structure (alpha/beta diversity, specific bacterial genera); (3) functional consequences including enhanced short-chain fatty acid production and tryptophan metabolism; (4) causal evidence from fecal microbiota transplantation; (5) correlations between microbiota changes and clinical improvement. Key findings reveal that acupuncture induces “convergent remodeling” of microbial structure toward a healthy profile, exerts “bidirectional regulation” on beneficial and harmful bacteria, and establishes a “niche selection” mechanism via neuro-immune pathways. These microbiota-mediated effects integrate with neural, endocrine, and immune pathways, forming a “point-to-surface” networked regulatory pattern that explains acupuncture’s dual efficacy in alleviating both gastrointestinal and psychological symptoms. This review provides a novel theoretical framework for understanding acupuncture’s therapeutic mechanisms and supports its clinical application in IBS management.

Without getting under your skin: non-invasive stimulation activates the vagus nerve

Cervical non-invasive vagus nerve stimulation (nVNS) has emerged as a practical neuromodulation approach with FDA-cleared indications in primary headache disorders, yet skepticism persists over whether transcutaneous stimulation can reliably engage vagal fibers or whether observed benefits reflect nonspecific cervical activation. Here, we synthesize converging anatomical, biophysical, physiological, and clinical evidence demonstrating that nVNS does, in fact, activate vagal pathways without surgical implantation. We first review cervical vagus anatomy and the biophysical basis for target engagement, including ultrasound-measured nerve depth and multi-scale computational models showing that clinically relevant stimulation can recruit predominantly large myelinated vagal fibers. We then integrate mechanistic evidence across complementary modalities: functional imaging consistently modulates canonical vagal projection sites (including brainstem nuclei), electrophysiology demonstrates peripheral vagal recruitment and centrally transmitted evoked responses, immune studies reveal reproducible suppression of pro-inflammatory cytokines consistent with cholinergic anti-inflammatory reflex engagement, and autonomic biomarkers show shifts toward increased parasympathetic tone. Finally, we contextualize these mechanistic findings with sham-controlled randomized trials in cluster headache and migraine, where nVNS repeatedly outperforms sham for acute and preventive outcomes with a favorable safety profile. Together, these independent lines of evidence form a coherent mechanistic fingerprint that is difficult to reconcile with placebo or superficial muscle stimulation accounts. We conclude that nVNS provides a credible, scalable means of accessing vagal neurophysiology and represents a clinically validated, paradigm-shifting advance in bioelectronic medicine.

Predicting early neurological deterioration in acute branch atheromatous disease without reperfusion therapy: a machine learning model

BackgroundAcute branch atheromatous disease (BAD) is one of the leading contributors to morbidity and disability in Asia, and early neurological deterioration (END) is common in affected patients. This study aimed to establish machine learning models to predict the risk of END in patients without reperfusion therapy.MethodsPatients with acute BAD who did not receive reperfusion therapy were retrospectively enrolled. Core predictive features were selected by LASSO regression with bootstrap stability assessment, and we used seven machine learning algorithms to build models. XGBoost was selected based on validation performance, nested cross-validation, and 1,000-iteration bootstrap validation. A spline logistic regression model served as the non-linear baseline. SHAP analysis was used to explain the model and develop a simple scoring system. Model discrimination was assessed using the area under the receiver operating characteristic curve (AUC), and clinical utility was evaluated using decision curve analysis (DCA).ResultsA total of 369 patients were included in our research. We screened predictive factors with LASSO regression and ultimately identified five key variables. These included maximum infarct area, lactate dehydrogenase (LDH), number of infarct slices, admission systolic blood pressure (SBP), and neutrophil count. The XGBoost model achieved the best overall performance, with AUC of 0.927 in the training set and 0.846 in the validation set. Nested cross-validation yielded an unbiased AUC of 0.866 (95% CI: 0.817–0.925), and bootstrap validation produced a mean OOB AUC of 0.855 (95% CI: 0.760–0.941). The scoring system stratified patients into low (0–6 points), intermediate (7–13 points), and high (14–20 points) risk groups. DCA demonstrated favorable clinical utility. SHAP analysis also indicated that maximum infarct area and LDH were the top two predictors of END.ConclusionAn XGBoost-based prediction model and a simple scoring system, integrating maximum infarct area, LDH, number of infarct slices, admission SBP, and neutrophil count, provide reliable END risk prediction for acute BAD patients without reperfusion therapy.