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GPD1L antibody (N-Term)

This anti-GPD1L antibody is a Rabbit Polyclonal antibody detecting GPD1L in WB, IHC (p) and EIA. Suitable for Human and Mouse.
Catalog No. ABIN952587

Quick Overview for GPD1L antibody (N-Term) (ABIN952587)

Target

See all GPD1L Antibodies
GPD1L (Glycerol-3-Phosphate Dehydrogenase 1-Like (GPD1L))

Reactivity

  • 28
  • 20
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human, Mouse

Host

  • 25
  • 3
Rabbit

Clonality

  • 27
  • 1
Polyclonal

Conjugate

  • 16
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This GPD1L antibody is un-conjugated

Application

  • 20
  • 13
  • 9
  • 9
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)
  • Binding Specificity

    • 8
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 47-77, N-Term

    Specificity

    This antibody reacts to GPD1L.

    Cross-Reactivity (Details)

    Species reactivity (tested):Human and Mouse.

    Purification

    Affinity chromatography on Protein A

    Immunogen

    KLH conjugated synthetic peptide between 47-77 amino acids from the N-terminal region of human GPD1L

    Isotype

    Ig Fraction
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.25 mg/mL

    Buffer

    PBS, 0.09 % (W/V) sodium azide

    Preservative

    Sodium azide

    Precaution of Use

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

    Handling Advice

    Avoid repeated freezing and thawing.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Target

    GPD1L (Glycerol-3-Phosphate Dehydrogenase 1-Like (GPD1L))

    Alternative Name

    GPD1L

    Background

    The protein encoded by this gene catalyzes the conversion of sn-glycerol 3-phosphate to glycerone phosphate. The encoded protein is found in the cytoplasm, associated with the plasma membrane, where it binds the sodium channel, voltage-gated, type V, alpha subunit (SCN5A). Defects in this gene are a cause of Brugada syndrome type 2 (BRS2) as well as sudden infant death syndrome (SIDS).Synonyms: GPD1-L, Glycerol-3-phosphate dehydrogenase 1-like protein, KIAA0089

    Molecular Weight

    38419 Da

    Gene ID

    23171

    NCBI Accession

    NP_055956
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