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>   home   >   Products   >   Primary Antibodies   >   HOXD9 Antibody (monoclonal) (M01)   

HOXD9 Antibody (monoclonal) (M01)

Mouse monoclonal antibody raised against a partial recombinant HOXD9.

  • WB - HOXD9 Antibody (monoclonal) (M01) AT2431a
    Antibody Reactive Against Recombinant Protein.Western Blot detection against Immunogen (33.15 KDa) .
  • WB - HOXD9 Antibody (monoclonal) (M01) AT2431a
    HOXD9 monoclonal antibody (M01), clone 2A9 Western Blot analysis of HOXD9 expression in NIH/3T3 ( (Cat # AT2431a )
Product Information
  • Applications Legend:
  • WB=Western Blot
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin-embedded Sections)
  • IHC-F=Immunohistochemistry (Frozen Sections)
  • IF=Immunofluorescence
  • FC=Flow Cytopmetry
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • IP=Immunoprecipitation
  • DB=Dot Blot
  • CHIP=Chromatin Immunoprecipitation
  • FA=Fluorescence Assay
  • IEM=Immunoelectronmicroscopy
  • EIA=Enzyme Immunoassay
Primary Accession P28356
Other Accession NM_014213
Reactivity Human, Mouse
Host mouse
Clonality Monoclonal
Isotype IgG1 Kappa
Clone Names 2A9
Calculated MW 36495 Da
Additional Information
Gene ID 3235
Other Names Homeobox protein Hox-D9, Homeobox protein Hox-4C, Homeobox protein Hox-52, HOXD9, HOX4C
Target/Specificity HOXD9 (NP_055028, 146 a.a. ~ 210 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
Dilution WB~~1:500~1000
Format Clear, colorless solution in phosphate buffered saline, pH 7.2 .
StorageStore at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
PrecautionsHOXD9 Antibody (monoclonal) (M01) is for research use only and not for use in diagnostic or therapeutic procedures.
Citations (0)

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This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXD genes located at 2q31-2q37 chromosome regions. Deletions that removed the entire HOXD gene cluster or 5' end of this cluster have been associated with severe limb and genital abnormalities. The exact role of this gene has not been determined.


Altered transmission of HOX and apoptotic SNPs identify a potential common pathway for clubfoot. Ester AR, et al. Am J Med Genet A, 2009 Dec. PMID 19938081.High-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older men. Yerges LM, et al. J Bone Miner Res, 2009 Dec. PMID 19453261.Mutations in HOXD13 underlie syndactyly type V and a novel brachydactyly-syndactyly syndrome. Zhao X, et al. Am J Hum Genet, 2007 Feb. PMID 17236141.Immunocytochemical detection of HoxD9 and Pbx1 homeodomain protein expression in Chinese esophageal squamous cell carcinomas. Liu DB, et al. World J Gastroenterol, 2005 Mar 14. PMID 15770739.[Increased expression of HOXA9 gene in Hirschsprung disease] M?chine-Neuville A, et al. Gastroenterol Clin Biol, 2002 Dec. PMID 12520199.

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$ 315.00
Cat# AT2431a
(40 western blots)
Availability: 7-10 days
Bulk Size
Seasonal Special on Bulk Order
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