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POMT1 antibody

This anti-POMT1 antibody is a Rabbit Polyclonal antibody detecting POMT1 in WB. Suitable for Human and Mouse.
Catalog No. ABIN6566852

Quick Overview for POMT1 antibody (ABIN6566852)

Target

See all POMT1 Antibodies
POMT1 (Protein-O-Mannosyltransferase 1 (POMT1))

Reactivity

  • 45
  • 5
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Mouse

Host

  • 48
Rabbit

Clonality

  • 48
Polyclonal

Conjugate

  • 21
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This POMT1 antibody is un-conjugated

Application

  • 27
  • 16
  • 15
  • 13
  • 13
  • 13
  • 7
  • 6
  • 6
  • 3
  • 1
Western Blotting (WB)
  • Purification

    Affinity purification

    Immunogen

    Recombinant protein of human POMT1

    Isotype

    IgG
  • Application Notes

    WB 1:1000 - 1:2000

    Restrictions

    For Research Use only
  • Concentration

    1 mg/mL

    Buffer

    Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    POMT1 (Protein-O-Mannosyltransferase 1 (POMT1))

    Alternative Name

    POMT1

    Background

    Synonyms: Dolichyl phosphate mannose protein mannosyltransferase 1,Dolichyl phosphate mannose protein mannosyltransferase1,Dolichyl-phosphate-mannose--protein mannosyltransferase 1,LGMD2K,MDDGA1,MDDGB1,MDDGC1,POMT 1,POMT1,POMT1,Protein O mannosyl transferase 1,Protein O mannosyl transferase1,Protein O-mannosyl-transferase 1,Rotate abdomen,Drosophila,homolog of,RT

    Background: The protein encoded by this gene is an O-mannosyltransferase that requires interaction with the product of the POMT2 gene for enzymatic function. The encoded protein is found in the membrane of the endoplasmic reticulum. Defects in this gene are a cause of Walker-Warburg syndrome (WWS) and limb-girdle muscular dystrophy type 2K (LGMD2K). Several transcript variants encoding different isoforms have been found for this gene.

    Molecular Weight

    Observed_MW: 53kDa

    Calculated_MW: 69kDa/76kDa/82kDa/84kDa

    Gene ID

    10585

    UniProt

    Q9Y6A1
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