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Transmembrane Protein 70 (TMM70) (AA 231-260), (C-Term) anticorps

Cet anticorps Lapin Polyclonal détecte spécifiquement dans WB et IHC (p). Il présente une réactivité envers Humain.
N° du produit ABIN656935

Aperçu rapide pour Transmembrane Protein 70 (TMM70) (AA 231-260), (C-Term) anticorps (ABIN656935)

Antigène

Voir toutes Transmembrane Protein 70 (TMM70) Anticorps
Transmembrane Protein 70 (TMM70)

Reactivité

  • 14
  • 3
  • 2
Humain

Hôte

  • 13
  • 1
Lapin

Clonalité

  • 13
  • 1
Polyclonal

Conjugué

  • 9
  • 1
  • 1
  • 1
  • 1
  • 1
Inconjugué

Application

  • 14
  • 10
  • 10
  • 4
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone

RB32747
  • Épitope

    • 7
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 231-260, C-Term

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogène

    This TMM70 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 231-260 amino acids from the C-terminal region of human TMM70.

    Isotype

    Ig Fraction
  • Indications d'application

    WB: 1:1000. IHC-P: 1:10~50

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 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.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    TMM70 Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

    Date de péremption

    6 months
  • Antigène

    Transmembrane Protein 70 (TMM70)

    Autre désignation

    TMM70

    Sujet

    This gene likely encodes a mitochondrial membrane protein. The encoded protein may play a role in biogenesis of mitochondrial ATP synthase. Mutations in this gene have been associated with neonatal mitochondrial encephalocardiomyopathy due to ATP synthase deficiency. Alternatively spliced transcript variants have been described.

    Poids moléculaire

    28969

    ID gène

    54968

    NCBI Accession

    NP_001035703, NP_060336

    UniProt

    Q9BUB7
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