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GLT25D1 antibody (AA 34-454)

This Rabbit Polyclonal antibody specifically detects GLT25D1 in WB, ELISA and FACS. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN7874081
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for GLT25D1 antibody (AA 34-454) (ABIN7874081)

Target

See all GLT25D1 Antibodies
GLT25D1 (Glycosyltransferase 25 Domain Containing 1 (GLT25D1))

Reactivity

Human, Mouse, Rat

Host

  • 5
Rabbit

Clonality

  • 5
Polyclonal

Conjugate

  • 5
This GLT25D1 antibody is un-conjugated

Application

  • 4
  • 3
  • 1
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • Binding Specificity

    • 1
    • 1
    • 1
    AA 34-454

    Purpose

    COLGALT1 Antibody / Collagen beta(1-O)galactosyltransferase 1

    Purification

    Immunogen affinity purified

    Immunogen

    E.coli-derived human COLGALT1 recombinant protein (Position: A34-D454) was used as the immunogen for the COLGALT1 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the COLGALT1 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL

    Buffer

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the COLGALT1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    GLT25D1 (Glycosyltransferase 25 Domain Containing 1 (GLT25D1))

    Alternative Name

    COLGALT1

    Background

    COLGALT1 antibody detects Collagen beta(1-O)galactosyltransferase 1, an enzyme that catalyzes the transfer of galactose to hydroxylysine residues in collagen. This post-translational modification is essential for proper collagen folding, stability, and secretion. COLGALT1 functions within the endoplasmic reticulum and Golgi apparatus and contributes to the biosynthesis of structurally mature collagen fibers. The COLGALT1 antibody is widely used in connective tissue, developmental, and fibrosis research to study collagen maturation, glycosylation, and extracellular matrix regulation.

    COLGALT1 is encoded by the COLGALT1 gene located on human chromosome 19p13.2. The protein is approximately 739 amino acids long and is a member of the galactosyltransferase family. It forms a functional complex with its homolog COLGALT2 and works sequentially with lysyl hydroxylase (PLOD family) enzymes to glycosylate hydroxylysine residues in collagen alpha chains. This process stabilizes triple helix formation and enhances collagen secretion and cross-linking.

    The COLGALT1 antibody detects an 85 kilodalton protein by western blot and shows perinuclear staining under immunofluorescence microscopy consistent with Golgi localization. COLGALT1 activity is required for the synthesis of type I, II, III, and IV collagens. Deficiency or mutation results in defective collagen glycosylation, leading to abnormal extracellular matrix assembly and diseases such as Ehlers-Danlos syndrome and osteogenesis imperfecta-like disorders.

    COLGALT1 expression is tightly regulated during development and tissue repair. Increased expression promotes collagen deposition in fibrotic tissues, whereas reduced expression leads to unstable collagen and tissue fragility. It also contributes to tumor stroma remodeling by enhancing extracellular matrix density and rigidity, influencing cancer cell migration and angiogenesis.

    As a key enzyme linking collagen biosynthesis and tissue integrity, COLGALT1 serves as a critical target for studying connective tissue disorders and fibrotic diseases. NSJ Bioreagents provides a validated COLGALT1 antibody optimized for its applications, supporting research into collagen glycosylation, fibrosis, and tissue regeneration.

    UniProt

    Q8NBJ5

    Pathways

    SARS-CoV-2 Protein Interactome
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