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HOXA9 antibody

This anti-HOXA9 antibody is a Rabbit Monoclonal antibody detecting HOXA9 in WB and IHC. Suitable for Human.
Catalog No. ABIN7267764

Quick Overview for HOXA9 antibody (ABIN7267764)

Target

See all HOXA9 Antibodies
HOXA9 (Homeobox A9 (HOXA9))

Reactivity

  • 44
  • 31
  • 15
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 44
  • 6
  • 2
Rabbit

Clonality

  • 46
  • 6
Monoclonal

Conjugate

  • 33
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
This HOXA9 antibody is un-conjugated

Application

  • 35
  • 20
  • 9
  • 5
  • 5
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Purpose

    HOXA9 Rabbit mAb

    Cross-Reactivity

    Human, Rat

    Characteristics

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant protein of human HOXA9.

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IHC,1:50 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    HOXA9 (Homeobox A9 (HOXA9))

    Alternative Name

    HOXA9

    Background

    In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. This gene is highly similar to the abdominal-B (Abd-B) gene of Drosophila. A specific translocation event which causes a fusion between this gene and the NUP98 gene has been associated with myeloid leukemogenesis. Read-through transcription exists between this gene and the upstream homeobox A10 (HOXA10) gene.,HOXA9, ABD-B, HOX1, HOX1.7, HOX1G, homeobox A9,Epigenetics & Nuclear Signaling,Transcription Factors,Stem Cells,Endothelial Progenitors,HOXA9

    Molecular Weight

    35kDa

    Gene ID

    3205

    UniProt

    P31269
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