CHST3 rabbit pAb
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CHST3 rabbit pAb
Background:
This gene encodes an enzyme which catalyzes the sulfation of chondroitin, a proteoglycan found in the extracellular matrix and most cells which is involved in cell migration and differentiation. Mutations in this gene are associated with spondylepiphyseal dysplasia and humerospinal dysostosis. [provided by RefSeq, Mar 2009]Description:
This gene encodes an enzyme which catalyzes the sulfation of chondroitin, a proteoglycan found in the extracellular matrix and most cells which is involved in cell migration and differentiation. Mutations in this gene are associated with spondylepiphyseal dysplasia and humerospinal dysostosis. [provided by RefSeq, Mar 2009],UniProt:
Q7LGC8Swiss Prot:
Q7LGC8Reactivity:
Human; Rat; MouseImmunogen:
Synthesized peptide derived from part region of human proteinClonality:
PolyclonalSource:
RabbitApplications:
WB; ELISAConcentration:
1 mg/mlDilution:
WB 1:500-2000 ELISA 1:5000-20000Molecular Weight:
52kDStorage Conditions:
-20°C/1 yearObserved Molecular Weight:
52kDFragment:
IgGSubcellular Location:
Golgi apparatus membrane ; Single-pass type II membrane protein .Gene ID (Human):
9469
