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GPD1L anticorps (N-Term)

Cet anticorps anti-GPD1L est un anticorps Lapin Polyclonal détectant GPD1L dans WB, IHC (p) et EIA. Adapté pour Humain et Souris.
N° du produit ABIN952587

Aperçu rapide pour GPD1L anticorps (N-Term) (ABIN952587)

Antigène

Voir toutes GPD1L Anticorps
GPD1L (Glycerol-3-Phosphate Dehydrogenase 1-Like (GPD1L))

Reactivité

  • 28
  • 20
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Humain, Souris

Hôte

  • 25
  • 3
Lapin

Clonalité

  • 27
  • 1
Polyclonal

Conjugué

  • 16
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp GPD1L est non-conjugé

Application

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

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

    Specificité

    This antibody reacts to GPD1L.

    Réactivité croisée (Details)

    Species reactivity (tested):Human and Mouse.

    Purification

    Affinity chromatography on Protein A

    Immunogène

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

    Isotype

    Ig Fraction
  • Indications d'application

    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

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

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

    Conseil sur la manipulation

    Avoid repeated freezing and thawing.

    Stock

    4 °C/-20 °C

    Stockage commentaire

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

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

    Autre désignation

    GPD1L

    Sujet

    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

    Poids moléculaire

    38419 Da

    ID gène

    23171

    NCBI Accession

    NP_055956
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