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Thermo Fisher Scientific B4GALT1 Polyclonal Antibody
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Thermo Fisher Scientific B4GALT1 Polyclonal Antibody

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Rabbit polyclonal antibody targeting human B4GALT1, validated for Western blot. Recognizes C-terminal synthetic peptide of B4GALT1. Supplied as unconjugated liquid form at 1 mg/mL. Suitable for glycoconjugate and lactose biosynthesis research.

카탈로그번호
PA539057
판매단위
pk
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마지막 업데이트 2025. 08. 02. 오전 09:22
Thermo Fisher Scientific PA539057 B4GALT1 Polyclonal Antibody 100 ug pk판매 단위 pk ·
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688,900원VAT 포함 757,790원

Thermo Fisher Scientific · Thermo Fisher Scientific B4GALT1 Polyclonal Antibody

Applications

Western Blot (WB)

  • Tested Dilution: 1:500–1:1,000

Product Specifications

항목 내용
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen A synthetic peptide derived from the C-terminal region of human B4GALT1
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Storage Conditions -20°C
Shipping Conditions Wet ice
RRID AB_2555649

Target Information

This gene is one of seven beta-1,4-galactosyltransferase (beta4GalT) genes. They encode type II membrane-bound glycoproteins that have exclusive specificity for the donor substrate UDP-galactose, transferring galactose in a beta1,4 linkage to acceptor sugars such as GlcNAc, Glc, and Xyl.
Each beta4GalT has a distinct role in the biosynthesis of various glycoconjugates and saccharide structures. As type II membrane proteins, they possess an N-terminal hydrophobic signal sequence that directs the protein to the Golgi apparatus and remains uncleaved as a transmembrane anchor.

By sequence similarity, beta4GalTs form four groups:

  • beta4GalT1 and beta4GalT2
  • beta4GalT3 and beta4GalT4
  • beta4GalT5 and beta4GalT6
  • beta4GalT7

This gene is unique among beta4GalT genes because it encodes an enzyme participating in both glycoconjugate and lactose biosynthesis.
In glycoconjugate biosynthesis, the enzyme adds galactose to N-acetylglucosamine residues of monosaccharides or glycoprotein carbohydrate chains.
In lactose biosynthesis, occurring in lactating mammary tissues, the enzyme forms a heterodimer with alpha-lactalbumin to catalyze the reaction:
UDP-galactose + D-glucose <=> UDP + lactose.
The two enzymatic forms result from alternate transcription initiation sites and post-translational processing.


For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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