Products Antibodies Monoclonal Antibodies Anti-Olig2 Rabbit Monoclonal Antibody for WB, ELISA - Q13516

Monoclonal Antibodies

Anti-Olig2 Rabbit Monoclonal Antibody for WB, ELISA - Q13516

Item Number : CM0010100

Price varies based on specs and customizations


Application
WB, ELISA
Cross Reactivity
Mouse, Rat
Protein Weight
32kDa
ISO & CE icon

Shipping:

Contact us to get shipping details Enjoy On-time Dispatch Guarantee.

View Specs

Why Choose Us

Easy ordering process, quality products, and dedicated support for your business success.

Easy Process Quality Assured Dedicated Support

Core Product Specifications and Parameters

Parameter Value
Product Name Olig2 Rabbit mAb
Remarks/Alias BHLHB1; OLIGO2; RACK17; PRKCBP2; bHLHe19; Olig2
Species Human
GeneID (Human) 10215
GeneID 10215
Immunogen Synthetic Peptide|A synthetic peptide corresponding to a sequence within amino acids 200-300 of human Olig2 (Q13516).
Source Rabbit
Category Monoclonal Antibodies
Application WB, ELISA
Cross Reactivity Mouse, Rat
SWISS Q13516
Protein Weight 32kDa
Shipping Ice bag

Biological Background: Olig2 Function and Localization

  • Olig2 is a class B basic helix-loop-helix (bHLH) transcription factor, also designated BHLHB1, bHLHe19, PRKCBP2, or RACK17, that binds DNA to regulate gene expression.
  • It is essential for oligodendrocyte and motor neuron specification in the spinal cord and for somatic motor neuron development in the hindbrain.
  • Olig2 cooperates with ZNF488 to drive oligodendrocyte differentiation and works alongside OLIG1 to establish the pMN progenitor domain of the embryonic neural tube.
  • During cortical development, it controls progenitor fate decisions in gliogenesis and contributes to gliomagenesis; it is classified as a proto-oncogene subject to chromosomal rearrangements.
  • The protein acts as a transcriptional repressor of GSX2 by binding and silencing multiple conserved enhancer elements, thereby suppressing olfactory bulb interneuron intermediate progenitor generation.
  • It is found in both the nucleus and the cytoplasm, consistent with its DNA-binding role and potential shuttling between compartments.
  • Olig2 is predominantly expressed in the brain, notably in oligodendrocytes; it is highly expressed in oligodendrogliomas, with variable levels in astrocytomas and glioblastomas.
  • Key post-translational modifications include ubiquitin-like conjugation, and the protein has been identified in proteomic screens.

Experimental Guidance and Technical Tips

  • The immunogen is a synthetic peptide from the internal region (aa 200–300) of human Olig2; the antibody is expected to recognize the full-length protein at ~32 kDa in Western blotting.
  • For WB, use lysates from human, mouse, or rat brain tissue or Olig2-expressing cell lines (e.g., oligodendroglioma) and validate with appropriate loading controls.
  • In ELISA, consider using the immunogen peptide or recombinant Olig2 protein as a standard and optimize coating conditions to ensure specificity.
  • Since the antibody cross-reacts with mouse and rat, it is suitable for comparative and cross-species studies; verify reactivity in your specific experimental system.

CamelBio: Your One-Stop Sourcing Bridge

CamelBio offers this anti-Olig2 monoclonal antibody as part of a comprehensive portfolio for oligodendrocyte differentiation and gliomagenesis research. We support diagnostic manufacturers and laboratories with validated antibody pairs, optimized monoclonal/polyclonal antibodies, bulk ancillary reagents, and custom raw-material sourcing. Our one-stop platform accelerates your transition from concept to clinic by providing dependable IVD components and technical expertise.

View more faqs for this product

REQUEST A QUOTE

Our professional team will reply to you within one business day. Please feel free to contact us!

Related Articles

Matrix Interference in ELISA Development: Designing Accuracy Into Complex-Sample Assays

Matrix Interference in ELISA Development: Designing Accuracy Into Complex-Sample Assays

Learn how to diagnose and control ELISA matrix interference through sample cleanup, buffer design, calibration, and smarter reagent selection.

Find out more

From Matrix Noise to Measurable Signal: A Practical Extraction Strategy for ELISA Testing

Learn how pentane extraction, alkaline back-extraction, and neutral buffering remove matrix effects before sensitive ELISA analysis.

Find out more

When the Dye Sees Everything: A Systematic Strategy for Cleaner, More Reliable qPCR

Learn how primer design, Mg2+ control, thermal optimization, and melt curves reduce background signal in dye-based qPCR assays.

Find out more

From Molecular Recognition to Reliable Results: Engineering Biosensors for Rapid Safety Testing

How antibodies and enzymes turn invisible molecular events into reliable biosensor signals, and how material quality determines test performance.

Find out more

Two Positive Controls, One Clear Answer: Isolating RT and PCR Failure in qRT-PCR Diagnostics

Learn how dual positive controls isolate reverse transcription and PCR failures, improve qRT-PCR reliability, and support compliant diagnostic workflows.

Find out more
Designing Hydrolysis Probes That Win the Kinetic Race in Real-Time PCR

Designing Hydrolysis Probes That Win the Kinetic Race in Real-Time PCR

Learn how probe Tm, primer spacing, sequence composition, and assay validation determine qPCR signal strength and diagnostic reliability.

Find out more

Specificity Is Built in Gates: A Hybridoma Screening Workflow for Reliable Immunoassay Raw Materials

A practical hybridoma screening workflow that removes carrier binders, proves native-target recognition, and limits cross-reactivity in IVD assays.

Find out more

qPCR Primer Design: The Small Decisions That Determine Assay Reliability

A practical guide to qPCR primer design, from amplicon length and 3' stability to validation for efficient, reproducible diagnostics.

Find out more

From Sorbent Bed to Antibody Signal: Designing SPE Workflows That Immunoassays Can Trust

Learn how pH, flow rate, washing, drying, and detergent-based reconstitution determine SPE recovery and immunoassay reliability.

Find out more

When a Surface Becomes a Sensor: Choosing Between QCM, SAW, and Six Classes of Quality Detection

Explore six sensor families, how QCM and SAW convert molecular binding into frequency shifts, and why surface chemistry determines diagnostic reliability.

Find out more

Why Scorpion Probes Turn a Single Base into a Confident Genotyping Decision

Explore how Scorpion probe architecture enables rapid, high-specificity allele discrimination in IVD genotyping assays.

Find out more

The Silent Well: How No Template Controls Protect Molecular Diagnostic Integrity

A practical guide to No Template Controls: how unexpected qPCR signals reveal contamination, reagent impurities, artifacts, and broken workflow controls.

Find out more