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Monoclonal Anti-SHOX2 antibody produced in mouse

SIGMA/WH0006474M1 - clone 1D1, purified immunoglobulin, buffered aqueous solution

Synonym: Anti-OG12; Anti-OG12X; Anti-OGI2X; Anti-SHOT; Anti-short stature homeobox 2

Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-WH0006474M1-100UG 100 µg
$524.00
1/EA
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Western Blotting Western Blot analysis of SHOX2 expression in transfected 293T cell line by SHOX2 monoclonal antibody, clone 1D1. Lanes Lane 1: SHOX2 transfected lysate (37.6 kDa). Lane 2: Non-transfected lysate.
Enhanced Validation-RNAi Western blot analysis of SHOX2 over-expressed 293 cell line, cotransfected with SHOX2 Validated Chimera RNAi. Blot probed with SHOX2 monoclonal antibody, clone 1D1. GAPDH (36.1 kDa) used as specificity and loading control.
Western Blotting SHOX2 monoclonal antibody, clone 1D1 Western Blot analysis of SHOX2 expression in PC-12.
Western Blotting QC Western Blot detection against Immunogen (35.42 kDa).
ELISA Detection limit for recombinant GST tagged SHOX2 is 1 ng/mL as a capture antibody.

 

antibody form purified immunoglobulin
antibody product type primary antibodies
biological source mouse
clone 1D1, monoclonal
conjugate unconjugated
form buffered aqueous solution
GenBank® accession no. NM_006884 
isotype IgG2aκ
Quality Level 100 
shipped in dry ice
species reactivity mouse, rat, human
storage temp. −20°C
technique(s) indirect ELISA: suitable
  western blot: 1-5 μg/mL
UniProt accession no. O60902 
Disclaimer: Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
General description: This gene is a member of the homeobox family of genes that encode proteins containing a 60-amino acid residue motif that represents a DNA binding domain. Homeobox genes have been characterized extensively as transcriptional regulators involved in pattern formation in both invertebrate and vertebrate species. Several human genetic disorders are caused by aberrations in human homeobox genes. This locus represents a pseudoautosomal homeobox gene that is thought to be responsible for idiopathic short stature, and it is implicated in the short stature phenotype of Turner syndrome patients. This gene is considered to be a candidate gene for Cornelia de Lange syndrome. Alternative splicing results in multiple transcript variants. (provided by RefSeq)
Immunogen: SHOX2 (NP_006875, 117 a.a. ~ 204 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.

Sequence
SPELKDRKDDAKGMEDEGQTKIKQRRSRTNFTLEQLNELERLFDETHYPDAFMREELSQRLGLSEARVQVWFQNRRAKCRKQENQLHK
Legal Information: GenBank is a registered trademark of United States Department of Health and Human Services
Physical form: Solution in phosphate buffered saline, pH 7.4
RIDADR NONH for all modes of transport
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Storage Temp. −20°C
UNSPSC 12352203

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