OLIG2 (Human) Matched Antibody Pair

Catalog # H00010215-AP51

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Size:1 Set
Price: USD $ 607.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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QC Test

Sandwich ELISA detection sensitivity ranging from approximately 729x to 3x dilution of the OLIG2 293T overexpression lysate (non-denatured).

  • Specification

    Product Description

    This antibody pair set comes with a matched antibody pair to detect and quantify the protein level of human OLIG2.

    Reactivity

    Human

    Interspecies Antigen Sequence

    Mouse (95); Rat (95)

    Quality Control Testing

    Standard curve using OLIG2 293T overexpression lysate (non-denatured) as an analyte.

    Sandwich ELISA detection sensitivity ranging from approximately 729x to 3x dilution of the OLIG2 293T overexpression lysate (non-denatured).

    Supplied Product

    Antibody pair set content:
    1. Capture antibody: mouse monoclonal anti-OLIG2 (100 ug)
    2. Detection antibody: rabbit purified polyclonal anti-OLIG2 (50 ug)
    *Reagents are sufficient for at least 3-5 x 96 well plates using recommended protocols.

    Storage Instruction

    Store reagents of the antibody pair set at -20°C or lower. Please aliquot to avoid repeated freeze thaw cycle. Reagents should be returned to -20°C storage immediately after use.

  • Applications

    ELISA Pair (Transfected lysate)

  • Gene Info — OLIG2

    Entrez GeneID

    10215

    Gene Name

    OLIG2

    Gene Alias

    BHLHB1, OLIGO2, PRKCBP2, RACK17, bHLHe19

    Gene Description

    oligodendrocyte lineage transcription factor 2

    Omim ID

    606386

    Gene Ontology

    Hyperlink

    Gene Summary

    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. [provided by RefSeq

    Other Designations

    OTTHUMP00000067569|OTTHUMP00000067570|basic domain, helix-loop-helix protein, class B, 1|human protein kinase C-binding protein RACK17|oligodendrocyte-specific bHLH transcription factor 2|protein kinase C binding protein 2

  • Interactome
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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