C1GALT1 polyclonal antibody (A01)
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Specification
Product Description
Mouse polyclonal antibody raised against a partial recombinant C1GALT1.
Immunogen
C1GALT1 (NP_064541, 264 a.a. ~ 363 a.a) partial recombinant protein with GST tag.
Sequence
ETFHPFVPEHHLIKGYLPRTFWYWNYNYYPPVEGPGCCSDLAVSFHYVDSTTMYELEYLVYHLRPYGYLYRYQPTLPERILKEISQANKNEDTKVKLGNP
Host
Mouse
Reactivity
Human
Interspecies Antigen Sequence
Mouse (89); Rat (92)
Quality Control Testing
Antibody Reactive Against Recombinant Protein.
Western Blot detection against Immunogen (37.11 KDa) .
Storage Buffer
50 % glycerol
Storage Instruction
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
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Applications
Western Blot (Cell lysate)
C1GALT1 polyclonal antibody (A01), Lot # 060109JC01 Western Blot analysis of C1GALT1 expression in HepG2 ( Cat # L019V1 ).Western Blot (Recombinant protein)
ELISA
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Gene Info — C1GALT1
Entrez GeneID
56913GeneBank Accession#
NM_020156Protein Accession#
NP_064541Gene Name
C1GALT1
Gene Alias
C1GALT, T-synthase
Gene Description
core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1
Omim ID
610555Gene Ontology
HyperlinkGene Summary
The common core 1 O-glycan structure Gal-beta-1-3GalNAc-R is a precursor for many extended mucin-type O-glycan structures in animal cell surface and secreted glycoproteins. Core 1 is synthesized by the transfer of Gal from UDP-Gal to GalNAc-alpha-1-R by core 1 beta-3-galactosyltransferase (C1GALT1) (Ju et al., 2002 [PubMed 11677243]).[supplied by OMIM
Other Designations
core 1 UDP-galactose:N-acetylgalactosamine-alpha-R beta 1,3-galactosyltransferase|core 1 beta3-Gal-T
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Interactome
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Pathway
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Disease
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Publication Reference
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Elevated expression of L-selectin ligand in lymph node-derived human prostate cancer cells correlates with increased tumorigenicity.
Radhakrishnan P, Lin MF, Cheng PW.
Glycoconjugate Journal 2008 Aug; 26(1):75.
Application:WB, Human, LNCaP cells.
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Elevated expression of L-selectin ligand in lymph node-derived human prostate cancer cells correlates with increased tumorigenicity.
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