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MMP26 anticorps (AA 96-125)

L’anticorps Lapin Polyclonal anti-MMP26 a été validé pour WB. Il convient pour détecter MMP26 dans des échantillons de Humain.
N° du produit ABIN5537136

Aperçu rapide pour MMP26 anticorps (AA 96-125) (ABIN5537136)

Antigène

Voir toutes MMP26 Anticorps
MMP26 (Matrix Metallopeptidase 26 (MMP26))

Reactivité

  • 38
  • 2
  • 2
  • 1
Humain

Hôte

  • 33
  • 5
Lapin

Clonalité

  • 32
  • 6
Polyclonal

Conjugué

  • 13
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp MMP26 est non-conjugé

Application

  • 32
  • 14
  • 13
  • 13
  • 3
  • 3
  • 1
Western Blotting (WB)
  • Épitope

    • 15
    • 7
    • 3
    • 3
    • 2
    • 1
    AA 96-125

    Purification

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

    Immunogène

    This MMP26 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 96-125 amino acids from the Central region of human MMP26.

    Isotype

    Ig Fraction
  • Indications d'application

    For WB starting dilution is: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5 mg/mL

    Buffer

    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

    Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
  • Antigène

    MMP26 (Matrix Metallopeptidase 26 (MMP26))

    Autre désignation

    MMP26

    Sujet

    Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Most MMP's are secreted as inactive proproteins which are activated when cleaved by extracellular proteinases. The encoded protein degrades type IV collagen, fibronectin, fibrinogen, casein, vitronectin, alpha 1-antitrypsin, alpha 2-macroglobulin, and insulin-like growth factor-binding protein 1, and activates MMP9 by cleavage. The protein differs from most MMP family members in that it lacks a conserved C-terminal protein domain.

    Poids moléculaire

    30 kDa

    ID gène

    56547

    UniProt

    Q9NRE1
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