B3GALT6 Antibody

Datasheet

Code	CSB-PA002494GA01HU
Size	$600
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Product Details
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Target Background

Product Details

Uniprot No.

Q96L58

Target Names

B3GALT6

Alternative Names

B3GALT6 antibody; Beta-1,3-galactosyltransferase 6 antibody; Beta-1,3-GalTase 6 antibody; Beta3Gal-T6 antibody; Beta3GalT6 antibody; EC 2.4.1.134 antibody; GAG GalTII antibody; Galactosyltransferase II antibody; Galactosylxylosylprotein 3-beta-galactosyltransferase antibody; UDP-Gal:betaGal beta 1,3-galactosyltransferase polypeptide 6 antibody

Raised in

Rabbit

Species Reactivity

Human,Mouse,Rat

Immunogen

Human B3GALT6

Immunogen Species

Homo sapiens (Human)

Isotype

IgG

Purification Method

Antigen Affinity purified

Concentration

It differs from different batches. Please contact us to confirm it.

Buffer

PBS with 0.02% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.

Tested Applications

ELISA,WB

Protocols

ELISA Protocol
Western Blotting(WB) Protocol

Troubleshooting and FAQs

Antibody FAQs

Storage

Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.

Lead Time

Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

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Target Background

Function

Beta-1,3-galactosyltransferase that transfers galactose from UDP-galactose to substrates with a terminal beta-linked galactose residue. Has a preference for galactose-beta-1,4-xylose that is found in the linker region of glycosaminoglycans, such as heparan sulfate and chondroitin sulfate. Has no activity towards substrates with terminal glucosamine or galactosamine residues.

Gene References into Functions

B3GALT6 encoding an enzyme involved in the biosynthesis of the GAG linker region is responsible for a severe skeletal dysplasia, spondyloepimetaphyseal dysplasia with joint laxity type 1. PMID: 23664117
Genetic association between B3GALT6 and Ehlers-Danlos-syndrome-like connective tissue disorder in 3 families. PMID: 23664118

Involvement in disease

Ehlers-Danlos syndrome, progeroid type, 2 (EDSP2); Spondyloepimetaphyseal dysplasia with joint laxity, 1, with or without fractures (SEMDJL1)

Subcellular Location

Golgi apparatus, Golgi stack membrane; Single-pass type II membrane protein.

Protein Families

Glycosyltransferase 31 family

Tissue Specificity

Ubiquitous.

Database Links

HGNC: 17978

OMIM: 271640

KEGG: hsa:126792

STRING: 9606.ENSP00000368496

UniGene: Hs.284284

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Protein Service

Gene Synthesis Service

Oligo Synthesis Service

Antibody FAQs What Is an Antibody? How to Choose an Antibody for Scientific Research? The difference between primary antibody and secondary antibod The Meaning of Irregular Antibody Screening Tag Antibodies, Your Good Partner in Protein Research How to Choose the Loading Control Antibodies?

Call us

301-363-4651 (Available 9 a.m. to 5 p.m. CST from Monday to Friday)

[email protected]

Address

7505 Fannin St., Ste 610, Room 7 (CUBIO Innovation Center), Houston, TX 77054, USA

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