TEL: +86 571 56623320    EMAIL: [email protected]

Rabbit Anti-B4GALT7 Polyclonal Antibody
Rabbit Anti-B4GALT7 Polyclonal Antibody
EDSP1; EDSSLA; EDSSPD1; XGALT1; XGPT; XGPT1; B4GT7_HUMAN; B4GALT7; Beta-1,4-GalTase 7; Beta4Gal-T7; b4Gal-T7; Proteoglycan UDP-galactose:beta-xylose beta1,4-galactosyltransferase I; UDP-Gal:beta-GlcNAc beta-1,4-galactosyltransferase 7; UDP-galactose:beta-
Total $295.0
(Vip priceV)
Regular members: $236.0
  • NO.:SLA0329
    concentration:1mg/ml
    React Species:Human, Mouse
    Immunogen Species:Rabbit
    Clonality:Polyclonal
    Applications:WB, ELISA
    Gene name:B4GALT7
    UniProt Entry:Q9UBV7
    NCBI Gene Entry:11285
  • Goods click count:11
  • Product Spec:
  • Quantity: - +
  • Limit points for buying:0 Points
  • Manual
  • Add to cart Inquiry Add to favorite
All categories

Details

 

Product NameRabbit Anti-B4GALT7 Polyclonal Antibody
Cat No.SLA0329
Chinese Name半乳糖转移酶7亚基β1,4抗体
AliasEDSP1; EDSSLA; EDSSPD1; XGALT1; XGPT; XGPT1; B4GT7_HUMAN; B4GALT7; Beta-1,4-GalTase 7; Beta4Gal-T7; b4Gal-T7; Proteoglycan UDP-galactose:beta-xylose beta1,4-galactosyltransferase I; UDP-Gal:beta-GlcNAc beta-1,4-galactosyltransferase 7; UDP-galactose:beta-N-acetylglucosamine beta-1,4-galactosyltransferase 7; UDP-galactose:beta-xylose beta-1,4-galactosyltransferase; XGalT-1; Xylosylprotein 4-beta-galactosyltransferase; Xylosylprotein beta-1,4-galactosyltransferase; 2.4.1.-; beta-1,4-galactosyltransferase 7; xylosylprotein beta 1,4-galactosyltransferase, polypeptide 7; galactosyltransferase I
Host SpeciesRabbit
IsotypeIgG
ClonalityPolyclonal
React SpeciesHuman,Mouse
ApplicationsWB (1:500-2000)
ELISA (1:5000-20000)
Not yet tested in other applications.
Optimal working dilutions must be determined by the end user.
ImmunogenKLH conjugated synthetic peptide derived from human B4GALT7
Purificationaffinity purified by Protein A
Concentration1mg/ml
Predicted MW.37 kDa
Observed MW.37 kDa
Subcellular LocationCytoplasm
Gene ID11285
Swiss-ProtQ9UBV7
Storage0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
Backgroundβ-1,4-galactosyltransferases (β-1,4-Gal-T) are type II membrane-bound glycoproteins that are substrate-specific and function to transfer galactose in a β-1,4 linkage to an acceptor sugar. There are seven members of the β-1,4-Gal-T family, all of which are directed to the golgi apparatus through a hydrophobic sequence at the N-terminus. β-1,4-Gal-T7, also known as B4GALT7 or XGALT1, is a 327 amino acid single-pass type II membrane protein that is expressed at high levels in heart, pancreas and liver. β-1,4-Gal-T7 uses manganese to catalyze the UDP-dependent biosynthesis of glycosphingolipids. The gene encoding β-1,4-Gal-T7 is mutated in Ehlers-Danlos syndrome progeroid type (EDSP), a variant form of Ehlers-Danlos syndrome characterized by progeroid facies, mild mental retardation, short stature, skin hyperextensibility, moderate skin fragility, joint hypermobility principally in digits.β-1,4-galactosyltransferases (β-1,4-Gal-T) are type II membrane-bound glycoproteins that are substrate-specific and function to transfer galactose in a ∫-1,4 linkage to an acceptor sugar. There are seven members of the β-1,4-Gal-T family, all of which are directed to the golgi apparatus through a hydrophobic sequence at the N-terminus. β-1,4-Gal-T7, also known as B4GALT7 or XGALT1, is a 327 amino acid single-pass type II membrane protein that is expressed at high levels in heart, pancreas and liver. β-1,4-Gal-T7 uses manganese to catalyze the UDP-dependent biosynthesis of glycosphingolipids. The gene encoding β-1,4-Gal-T7 is mutated in Ehlers-Danlos syndrome progeroid type (EDSP), a variant form of Ehlers-Danlos syndrome characterized by progeroid facies, mild mental retardation, short stature, skin hyperextensibility, moderate skin fragility, joint hypermobility principally in digits.-1,4-galactosyltransferases (β-1,4-Gal-T) are type II membrane-bound glycoproteins that are substrate-specific and function to transfer galactose in a ∫-1,4 linkage to an acceptor sugar. There are seven members of the β-1,4-Gal-T family, all of which are directed to the golgi apparatus through a hydrophobic sequence at the N-terminus. β-1,4-Gal-T7, also known as B4GALT7 or XGALT1, is a 327 amino acid single-pass type II membrane protein that is expressed at high levels in heart, pancreas and liver. β-1,4-Gal-T7 uses manganese to catalyze the UDP-dependent biosynthesis of glycosphingolipids. The gene encoding β-1,4-Gal-T7 is mutated in Ehlers-Danlos syndrome progeroid type (EDSP), a variant form of Ehlers-Danlos syndrome characterized by progeroid facies, mild mental retardation, short stature, skin hyperextensibility, moderate skin fragility, joint hypermobility principally in digits.
AttentionThis product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

 

FOR RESEARCH USE ONLY. Not for use in diagnostic or therapeutic procedures.

Partial purchase records(bought amounts latest0)

No one bought this product
Total 0 records, divided into1 pages First Prev Next Last

User Comment(Total0User Comment Num)

  • No comment
Total 0 records, divided into1 pages First Prev Next Last
Username: Anonymous user
E-mail:
Rank:
Content:
Verification code: captcha

Call us

+86 571 56623320

Address

Room 1-315, Kongle Changqing Building, No. 160 Guangye Road,Gongshu District, Hangzhou City, Zhejiang Province, China

Join Us with

Leave a message
* To protect against spam, please pass the CAPTCHA test below.
© 2005-2026 SUNLONG BIOTECH CO., LTD Copyright, All Rights Reserved.