PIPA523456

OLIG2 Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA523456-Each-of-1 In Stock ₹ 51,976.00

PIPA523456 - Each of 1

₹ 51,976.00

In Stock

Quantity

1

Base Price: ₹ 51,976.00

GST (18%): ₹ 9,355.68

Total Price: ₹ 61,331.68

Antigen

OLIG2

Classification

Polyclonal

Conjugate

Unconjugated

Gene

OLIG2

Gene Alias

AI604895; basic domain, helix-loop-helix protein, class B, 1; Basic helix loop helix protein class B1 (bHLHB1); basic helix-loop-helix protein 19 (bHLHe19); bHLH transcription factor; BHLHB1; bHLHe19; Class B basic helix-loop-helix protein 1; class E basic helix-loop-helix protein 19; human protein kinase C-binding protein RACK17; Olg-2; OLIG2; olig-2; Oligo2; Oligo2 antibody; oligodendrocyte lineage transcription factor 2; Oligodendrocyte specific bHLH transcription factor 2; oligodendrocyte transcription factor 2; oligodendrocyte-specific bHLH transcription factor 2; PRKCBP2; Protein kinase C-binding protein 2; Protein kinase C-binding protein 2 (PRKCBP2); Protein kinase C-binding protein RACK17; RACK17; RK17; wu:fc64g09

Host Species

Rabbit

Purification Method

Protein A

Regulatory Status

RUO

Gene ID (Entrez)

10215, 50913

Content And Storage

Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.

Form

Liquid

Applications

Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot

Concentration

1 mg/mL

Formulation

PBS with 0.05% sodium azide

Gene Accession No.

Q13516, Q9EQW6

Gene Symbols

OLIG2

Immunogen

A portion of amino acids 70-130 of human OLIG2 was used as the immunogen for the antibody.

Quantity

100 μg

Primary or Secondary

Primary

Target Species

Human, Mouse

Product Type

Antibody

Isotype

IgG

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Description

  • Description This gene encodes a basic helix-loop-helix transcription factor which is expressed in oligodendroglial tumors of the brain
  • The protein is an essential regulator of ventral neuroectodermal progenitor cell fate
  • The gene is involved in a chromosomal translocation t(14;21)(q11.2;q22) associated with T-cell acute lymphoblastic leukemia
  • Its chromosomal location is within a region of chromosome 21 which has been suggested to play a role in learning deficits associated with Down syndrome
  • Tissue specificity: Expressed in the brain, in oligodendrocytes
  • Strongly expressed in oligodendrogliomas, while expression is weak to moderate in astrocytomas
  • Expression in glioblastomas highly variable.