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SCCPDH anticorps

L’anticorps Lapin Polyclonal anti-SCCPDH a été validé pour WB, IHC et ELISA. Il convient pour détecter SCCPDH dans des échantillons de Humain, Souris et Rat.
N° du produit ABIN7247165

Aperçu rapide pour SCCPDH anticorps (ABIN7247165)

Antigène

Voir toutes SCCPDH Anticorps
SCCPDH (Saccharopine Dehydrogenase (SCCPDH))

Reactivité

  • 17
  • 11
  • 10
  • 3
  • 3
  • 2
  • 2
  • 1
Humain, Souris, Rat

Hôte

  • 15
  • 2
Lapin

Clonalité

  • 17
Polyclonal

Conjugué

  • 10
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp SCCPDH est non-conjugé

Application

  • 10
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogène

    Fusion protein of human SCCPDH

    Isotype

    IgG
  • Indications d'application

    WB 1:1000-1:5000, IHC 1:50-1:300, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1.5 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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.

    Stock

    -20 °C

    Stockage commentaire

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

    SCCPDH (Saccharopine Dehydrogenase (SCCPDH))

    Autre désignation

    SCCPDH

    Sujet

    SCCPDH (Probable saccharopine dehydrogenase) is a 429 amino acid protein that belongs to the saccharopine dehydrogenase family. The SCCPDH gene is conserved in chimpanzee, dog, cow, mouse, rat, chicken, fruit fly, mosquito and C.elegans, and maps to human chromosome 1q44. Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.

    Poids moléculaire

    Observed_MW: Refer to figures

    Calculated_MW: 47 kDa

    UniProt

    Q8NBX0

    Pathways

    SARS-CoV-2 Protein Interactome
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