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Render Timestamp: 2024-07-26T10:32:47.139Z
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PDP - Template Name: Monoclonal Antibody
PDP - Template ID: *******c5e4b77
R Recombinant
Recombinant: Superior lot-to-lot consistency, continuous supply, and animal-free manufacturing.

HOXB9 (E7P5O) Rabbit mAb #27967

Filter:
  • WB
  • IP
  • IF
  • F

    Supporting Data

    REACTIVITY H Mk
    SENSITIVITY Endogenous
    MW (kDa) 28
    Source/Isotype Rabbit IgG
    Application Key:
    • WB-Western Blotting 
    • IP-Immunoprecipitation 
    • IF-Immunofluorescence 
    • F-Flow Cytometry 
    Species Cross-Reactivity Key:
    • H-Human 
    • Mk-Monkey 

    Product Information

    Product Usage Information

    Application Dilution
    Western Blotting 1:1000
    Immunoprecipitation 1:100
    Immunofluorescence (Immunocytochemistry) 1:400 - 1:1600
    Flow Cytometry (Fixed/Permeabilized) 1:800 - 1:1600

    Storage

    Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/ml BSA, 50% glycerol and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody.

    Protocol

    Specificity / Sensitivity

    HOXB9 (E7P5O) Rabbit mAb recognizes endogenous levels of total HOXB9 protein. This antibody does not cross-react with HOXA9, HOXC9, or HOXD9 proteins.


    Species Reactivity:

    Human, Monkey

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Val116 of human HOXB9 protein.

    Background

    HOXB9 is a member of the HOXB gene cluster which, along with the HOXA, HOXC, and HOXD gene clusters, governs embryonic patterning along the cranio-caudal axis (1,2). HOXB9 protein functions to regulate formation of the rib cage and contributes to development of the forelimbs (3,4). De-regulation of HOXB9 protein expression is associated with multiple types of cancer. HOXB9 expression is downregulated in pancreatic ductal adenocarcinoma and upregulated in lung adenocarcinoma, where it is associated with poor prognosis (5,6). Overexpression of HOXB9 in breast and hepatocellular carcinomas activates the epithelial-to-mesenchymal transition (EMT) through modulation of TGF-β, promoting tumor progression and metastasis (7,8). HOXB9 overexpression in gliomas increases tumorigenicity by stimulating proliferation, migration, and sphere formation (9).

      For Research Use Only. Not For Use In Diagnostic Procedures.
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