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  • Accession
  • Catalog #

HOXD9 Antibody (monoclonal) (M01)Purified Mouse Monoclonal Antibody (Mab)

Country
United States
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Ordering Information
Catalog # Size Availability Price  
AT2431a 100 ug 400 ul 7-10 days $ 315.00 Add to cart
  • Specification
  • Citiations : 0
  • Reviews
  • Protocols
  • Backgrounds

HOXD9 Antibody (monoclonal) (M01) - Product info

ApplicationWB
  • Applications Legend:
  • W=Western Blotting
  • IP=Immunoprecipitation
  • IHC-P=Immunohistochemistry (Paraffin)
  • IF-IC=Immunofluorescence (Immunocytochemistry)
  • F=Flow Cytometry
Primary AccessionP28356
Other AccessionNP_055028
ReactivityHuman
IsotypeIgG1 Kappa
Clone Names2A9
Calculated MW36495 Da

HOXD9 Antibody (monoclonal) (M01) - Additional info

Gene ID 3235
Other Names
HOX4, HOX4C, Hox4.3, Hox5.2homeobox D9
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 .
Storage
Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Precautions
HOXD9 Antibody (monoclonal) (M01) is for research use only and not for use in diagnostic or therapeutic procedures.

HOXD9 Antibody (monoclonal) (M01) - Application data

  • HOXD9 monoclonal antibody (M01), clone 2A9 Western Blot analysis of HOXD9 expression in NIH/3T3 ( Cat # L018V1 ).

HOXD9 Antibody (monoclonal) (M01) - Related products

RI12555: HOXD9 predesign siRNA

AT2431a: HOXD9 Antibody (monoclonal) (M01)

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Provided below are standard protocols that you may find useful for product applications.

BACKGROUND

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.

REFERENCES

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.