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MYORG/KIAA1161 antibody (AA 207-611)

The Rabbit Polyclonal anti-MYORG/KIAA1161 antibody is suitable to detect MYORG/KIAA1161 in samples from Human, Mouse and Rat. It has been validated for ELISA, WB and FACS.
Catalog No. ABIN7872108
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for MYORG/KIAA1161 antibody (AA 207-611) (ABIN7872108)

Target

See all MYORG/KIAA1161 (MYORG) Antibodies
MYORG/KIAA1161 (MYORG) (Myogenesis Regulating Glycosidase (MYORG))

Reactivity

Human, Mouse, Rat

Host

  • 8
Rabbit

Clonality

  • 8
Polyclonal

Conjugate

  • 4
  • 2
  • 1
  • 1
This MYORG/KIAA1161 antibody is un-conjugated

Application

  • 5
  • 3
  • 2
  • 1
  • 1
ELISA, Western Blotting (WB), Flow Cytometry (FACS)
  • Binding Specificity

    • 5
    • 1
    • 1
    AA 207-611

    Purpose

    MYORG Antibody / Myogenesis-regulating glycosidase

    Purification

    Immunogen affinity purified

    Immunogen

    E.coli-derived human MYORG recombinant protein (Position: Q207-R611) was used as the immunogen for the MYORG antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the MYORG 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 MYORG 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

    MYORG/KIAA1161 (MYORG) (Myogenesis Regulating Glycosidase (MYORG))

    Alternative Name

    MYORG

    Background

    MYORG antibody detects Myogenesis-regulating glycosidase, a lysosomal and endoplasmic reticulum-associated enzyme involved in protein processing and neurological function. The UniProt recommended name is Myogenesis-regulating glycosidase (MYORG). This glycosidase is highly conserved and plays a crucial role in the maintenance of glycoprotein homeostasis within neural tissues, particularly astrocytes.

    Functionally, MYORG antibody identifies a 714-amino-acid glycosidase belonging to the glycosyl hydrolase family 31. MYORG hydrolyzes terminal sugar residues from oligosaccharides and glycoproteins, participating in lysosomal degradation and protein quality control. It is mainly localized to the endoplasmic reticulum and perinuclear regions, suggesting involvement in post-translational processing rather than extracellular digestion.

    The MYORG gene is located on chromosome 9p13.1 and is highly expressed in brain and skeletal muscle. In the central nervous system, MYORG supports astrocyte differentiation and intercellular communication. It is co-regulated with genes controlling lysosomal activity, endoplasmic reticulum homeostasis, and metabolic signaling.

    Pathologically, mutations in MYORG cause primary familial brain calcification (PFBC), a neurodegenerative disorder characterized by calcium deposits in basal ganglia and cerebellum. Deficiency in MYORG leads to altered glycosylation and impaired protein turnover in astrocytes. Research using MYORG antibody assists studies of glycoprotein metabolism, lysosomal function, and neurological disease mechanisms.

    MYORG antibody is validated for western blotting, immunofluorescence, and immunohistochemistry to detect intracellular glycosidases and neuronal processing enzymes. NSJ Bioreagents provides MYORG antibody reagents optimized for neuroscience, enzymology, and cellular metabolism research.

    Structurally, Myogenesis-regulating glycosidase contains a catalytic domain typical of glycosyl hydrolases with conserved acid-base residues, and a C-terminal transmembrane region anchoring it to intracellular membranes. This antibody supports analysis of MYORG's biochemical function and contribution to neurodegenerative disorders.

    UniProt

    Q6NSJ0

    Pathways

    Skeletal Muscle Fiber Development
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