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POMT1 antibody

This anti-POMT1 antibody is a Rabbit Polyclonal antibody detecting POMT1 in WB. Suitable for Human.
Catalog No. ABIN7467653

Quick Overview for POMT1 antibody (ABIN7467653)

Target

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

Reactivity

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  • 6
  • 3
  • 2
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  • 1
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  • 1
Human

Host

  • 48
Rabbit

Clonality

  • 48
Polyclonal

Conjugate

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  • 1
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  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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  • 1
This POMT1 antibody is un-conjugated

Application

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Western Blotting (WB)
  • Cross-Reactivity

    Human

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein encompassing a sequence within the center region of human POMT1. The exact sequence is proprietary.

    Isotype

    IgG
  • Application Notes

    WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.79 mg/mL

    Buffer

    0.1M Tris-Glycine ( pH 7), 20 % Glycerol, 0.01 % Thimerosal

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • Target

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

    Alternative Name

    protein O-mannosyltransferase 1

    Background

    Protein O-mannosyltransferase 1 , LGMD2K , LGMDR11 , MDDGA1 , MDDGB1 , MDDGC1 , RT,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

    85 kDa

    Gene ID

    10585

    UniProt

    Q9Y6A1
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