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TPM2 anticorps (C-Term)

Cet anticorps anti-TPM2 est un anticorps Lapin Polyclonal détectant TPM2 dans WB. Adapté pour Humain.
N° du produit ABIN1536948

Aperçu rapide pour TPM2 anticorps (C-Term) (ABIN1536948)

Antigène

Voir toutes TPM2 Anticorps
TPM2 (Tropomyosin-2 (TPM2))

Reactivité

  • 56
  • 29
  • 12
  • 5
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 52
  • 6
Lapin

Clonalité

  • 52
  • 6
Polyclonal

Conjugué

  • 21
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp TPM2 est non-conjugé

Application

  • 40
  • 17
  • 13
  • 13
  • 13
  • 8
  • 6
  • 5
  • 4
  • 4
  • 1
  • 1
Western Blotting (WB)

Clone

RB20863
  • Épitope

    • 15
    • 7
    • 5
    • 3
    • 2
    • 1
    • 1
    • 1
    AA 252-280, C-Term

    Homologie

    B, C, M, Rb, Rat

    Purification

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

    Immunogène

    This TPM2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 252-280 amino acids from the C-terminal region of human TPM2.

    Isotype

    Ig Fraction
  • Indications d'application

    WB: 1:1000

    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

    TPM2 Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

    Date de péremption

    6 months
  • Antigène

    TPM2 (Tropomyosin-2 (TPM2))

    Autre désignation

    TPM2

    Sujet

    This gene encodes beta-tropomyosin, a member of the actin filament binding protein family, and mainly expressed in slow, type 1 muscle fibers. Mutations in this gene can alter the expression of other sarcomeric tropomyosin proteins, and cause cap disease, nemaline myopathy and distal arthrogryposis syndromes. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

    Poids moléculaire

    32851

    ID gène

    7169

    NCBI Accession

    NP_003280, NP_998839

    UniProt

    P07951
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