B3GALT6 purified MaxPab mouse polyclonal antibody (B01P)
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More Files
- More Functions
Immunofluorescence
Immunofluorescence of purified MaxPab antibody to B3GALT6 on HeLa cell. [antibody concentration 20 ug/ml]
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Specification
Product Description
Mouse polyclonal antibody raised against a full-length human B3GALT6 protein.
Immunogen
B3GALT6 (AAI60034.1, 1 a.a. ~ 329 a.a) full-length human protein.
Sequence
MKLLRRAWRRRAALGLGTLALCGAALLYLARCAAEPGDPRAMSGRSPPPPAPARAAAFLAVLVASAPRAAERRSVIRSTWLARRGAPGDVWARFAVGTAGLGAEERRALEREQARHGDLLLLPALRDAYENLTAKVLAMLAWLDEHVAFEFVLKADDDSFARLDALLAELRAREPARRRRLYWGFFSGRGRVKPGGRWREAAWQLCDYYLPYALGGGYVLSADLVHYLRLSRDYLRAWHSEDVSLGAWLAPVDVQREHDPRFDTEYRSRGCSNQYLVTHKQSLEDMLEKHATLAREGRLCKREVQLRLSYVYDWSAPPSQCCQRREGIP
Host
Mouse
Reactivity
Human
Interspecies Antigen Sequence
Mouse (83); Rat (84)
Quality Control Testing
Antibody reactive against mammalian transfected lysate.
Storage Buffer
In 1x PBS, pH 7.4
Storage Instruction
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
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Applications
Western Blot (Transfected lysate)
Western Blot analysis of B3GALT6 expression in transfected 293T cell line () by B3GALT6 MaxPab polyclonal antibody.
Lane 1: B3GALT6 transfected lysate(36.19 KDa).
Lane 2: Non-transfected lysate.
Immunofluorescence
Immunofluorescence of purified MaxPab antibody to B3GALT6 on HeLa cell. [antibody concentration 20 ug/ml] -
Gene Info — B3GALT6
Entrez GeneID
126792GeneBank Accession#
BC160034.1Protein Accession#
AAI60034.1Gene Name
B3GALT6
Gene Alias
beta3GalT6
Gene Description
UDP-Gal:betaGal beta 1,3-galactosyltransferase polypeptide 6
Gene Ontology
HyperlinkGene Summary
O
Other Designations
OTTHUMP00000001756|UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 6|beta-1,3-galactosyltransferase-6
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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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Biallelic B3GALT6 mutations cause spondylodysplastic Ehlers-Danlos syndrome.
Van Damme T, Pang X, Guillemyn B, Gulberti S, Syx D, De Rycke R, Kaye O, de Die-Smulders CEM, Pfundt R, Kariminejad A, Nampoothiri S, Pierquin G, Bulk S, Larson AA, Chatfield KC, Simon M, Legrand A, Gerard M, Symoens S, Fournel-Gigleux S, Malfait F.
Human Molecular Genetics 2018 Jun; [Epub].
Application：ICC, WB, Human, Human dermal fibroblasts.
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Defective Initiation of Glycosaminoglycan Synthesis due to B3GALT6 Mutations Causes a Pleiotropic Ehlers-Danlos Syndrome-like Connective Tissue Disorder.
Malfait F, Kariminejad A, Van Damme T, Gauche C, Syx D, Merhi-Soussi F, Gulberti S, Symoens S, Vanhauwaert S, Willaert A, Bozorgmehr B, Kariminejad MH, Ebrahimiadib N, Hausser I, Huysseune A, Fournel-Gigleux S, De Paepe A.
American Journal of Human Genetics 2013 Jun; 92(6):935.
Application：IF, Human, Fibroblast cells.
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Biallelic B3GALT6 mutations cause spondylodysplastic Ehlers-Danlos syndrome.
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