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Webinars and Training

Exploring Methodologies for Spatial Biology, from IF to IHC to multiplex IHC with SignalStar® Technology

March 5, 2026

Multiplex spatial biology enables the simultaneous detection of multiple protein targets, revealing cellular dynamics within their native spatial context and leading to a more comprehensive understanding of complex biological processes and systems.

In this seminar, we will provide a comprehensive overview of the basic immunodetection techniques necessary for spatial biology, namely Immunohistochemistry (IHC) and Immunofluorescence (IF).

Presented by: Flora Guarnotta, MSc Field Application Specialist at CST

Advancing Proteomics: Deep Profiling of Post-Translational Modifications (PTMSs) with PTMScan® Technology

March 26, 2026

Have you considered how post-translational modifications (PTMs) orchestrate cell signaling and function? PTMs like phosphorylation, ubiquitination, and acetylation are crucial regulatory switches. However, their low abundance and complexity have historically made global profiling a significant challenge.

To address this challenge, this seminar will provide you with an overview of proteomics research, which combines Global Protein and PTM Protein analysis.

Specifically, we will introduce you to PTMScan technology—a cutting-edge, mass spectrometry-based methodology. This technology uses proprietary PTM-specific antibodies to enrich, selectively isolate, and identify up to thousands of modified peptides in a single experiment.

Presented by: Yannick Nossin, PhD Field Application Scientist at CST

Accelerating Epigenomic Discovery: Chromatin Profiling Through CUT&RUN and CUT&Tag

April 23, 2026

Have you heard of CUT&RUN and CUT&Tag? These next-generation chromatin profiling technologies enable high-resolution mapping of DNA-binding proteins, histone modifications, and chromatin accessibility with exceptional sensitivity and low input requirements. In this seminar, you will learn how CUT&RUN and CUT&Tag work, the distinct advantages each method offers, and the key experimental considerations that guide the choice between them.

Join us to deepen your understanding of these powerful enzymatic profiling approaches and discover how they can help you unravel complex epigenetic regulation and accelerate your own scientific discoveries.

Presented by: Christina Theisgen, PhD Sr. Global Trainer at CST

Redefining Single-Cell Analysis: Comprehensive Intracellular Protein Profiling with InTraSeqâ„¢ Technology

May 28, 2026

Are you looking to capture the full picture of cellular signaling and gene expression at the single-cell level? Traditional single-cell sequencing often focuses on whole-cell transcripts or surface markers, missing the crucial intracellular dynamics orchestrated by proteins and their modifications.

This seminar focuses on InTraSeqTM Single Cell Analysis (Intracellular Protein and Transcriptomic Sequencing), a technology from CST that allows for the simultaneous detection of both RNA transcripts and intracellular proteins (including transcription factors and PTMs) from the same single cell.

Attend this session to understand the mechanics of InTraSeq Technology, see how its ability to integrate protein state (like phosphorylation) with gene expression within individual cells unlocks unprecedented insights into signaling heterogeneity, and learn how to leverage this technology to push the boundaries of single-cell biology.

Presented by: Yannick Nossin, PhD Field Application Scientist at CST

Latest Blog

Air-liquid interface culture: Building physiologically relevant airway models

Traditional cell culture systems often fall short of replicating the complex environment of the human airway, limiting their predictive power in respiratory research. To address these limitations, researchers increasingly rely on physiologically relevant in vitro models that better reflect human airway biology. Among these, air-liquid interface (ALI) culture bridges the gap between simple two-dimensional systems and complex animal models, offering a human-based approach for studying respiratory function and disease in vitro.

New Products this month from CST!

NG2/CSPG4 (F8X3M) Rabbit
Monoclonal Antibody #54851

IF-F: Confocal IF analysis of fixed mouse cerebellum labeled with #54851 (green), TMEM119 (E4B9S) Mouse Monoclonal Antibody #98778 (red), and ProLong Gold Antifade Reagent with DAPI #8961 (blue).

Proteoglycan Involved in Cell Scaffolding and Signaling

NG2 is a transmembrane chondroitin sulfate proteoglycan present on the cell surface. It promotes cell proliferation, migration, and metastasis through phosphorylation by PKCα and ERK. It is also expressed in vascular pericytes to regulate angiogenesis, and in the nervous system, it is involved in myelin repair as a marker of oligodendrocyte precursor cells. It is highly expressed in intractable cancers such as melanoma, glioblastoma, and triple-negative breast cancer, and is associated with treatment resistance and metastasis. Taking advantage of its unique expression pattern, NG2 is currently being clinically applied as a promising target for cancer immunotherapy, such as CAR-T cell therapy. #54851 is suitable for WB, IP, IF-F, IF-IC, FC-FP, and FC-L analysis using human, mouse, and rat samples.

BRD9 (F6F1S) Rabbit Monoclonal
Antibody #98202

ChIP: ChIP were performed with cross-linked chromatin from NIH/3T3 cells and either #98202 or Normal Rabbit IgG #2729, using SimpleChIP® Plus Enzymatic Chromatin IP Kit (Magnetic Beads) #9005. The enriched DNA was quantified by real-time PCR, using human RCN3 promoter primers, human ZFP948 intron 1 primers, and SimpleChIP® Mouse Intracisternal A-Particle (IAP) LTR Primers #85916. The amount of immunoprecipitated DNA in each sample is represented as signal relative to the total amount of input chromatin, which is equivalent to one.

Chromatin Remodeling Component

BRD9, a component of the non-canonical BAF complex, recognizes acetylated histones via its bromodomain and targets the complex to specific gene promoters and enhancers. BRD9 is particularly involved in maintaining stem cell pluripotency, cell differentiation, and regulating immune responses, regulating the expression of genes essential for cell fate determination. It has also been reported to be essential for tumor survival in synovial sarcoma and malignant rhabdoid tumors, which possess characteristic gene fusions. BRD9 is also involved in the proliferation of acute myeloid leukemia (AML), and in recent years, development of drugs targeting BRD9, such as PROTACs (targeted protein degradation inducers), has been progressing. #98202 is suitable for WB, IP, and ChIP using mouse and rat samples.

New Products This Month from NEB!

Fragmenting genomic DNA (gDNA) is key to improving long-read sequencing performance and data yield. NEBNext UltraShear® Long Read is a fast, flexible enzymatic method for gDNA fragmentation, designed for use upstream of Oxford Nanopore Technologies® (ONT) and PacBio® library preparation and sequencing. This time-tunable solution allows precise fragment sizing from 2 kb to 30 kb in as little as 30 minutes, while preserving native methylation marks. It works with a broad input range (250 ng–5 µg) and is compatible with automation, making it easy to scale as sequencing needs grow. NEBNext UltraShear Long Read provides a cost-effective and reliable alternative to mechanical shearing methods.

For Research Use Only. Not for use in diagnostic procedures.

  • Magnetic bead-based extraction for efficient and reproducible isolation of circulating cell-free DNA (cfDNA) from biofluids.
  • Recover cell-free DNA in the typical size range (150-300 bp), and as low as 50 bp.
  • Obtain consistent results for sample types with challenging biological variability.
  • Available in 20-prep or 100-prep formats for 2 ml samples and scalable to accommodate 1-4 ml sample inputs.
  • Elute in low elution volumes without the need for additional concentration steps that lead to yield loss.
  • Achieve streamlined sample-to-result workflows by integrating with NEB’s sequencing and amplification solutions.

Supercoiled Extend DNA Ladder enables accurate sizing of a wide range of supercoiled DNA, including supercoiled plasmids up to 15 kb, and has a convenient reference band at 6 kb.

  • Supercoiled DNA molecular weight marker
  • Size range: 2 to 15 kb
  • Convenient reference band at 6 kb
  • Supplied with a vial of Gel Loading Dye, Purple (6X), no SDS (NEB #B7025)
  • Suitable for 100 gel lanes

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