MMP2 anticorps (AA 193-545)

N° du produit ABIN1886151

Cet anticorps anti-MMP2 est un anticorps Lapin Polyclonal détectant MMP2 dans WB et IF. Adapté pour Humain.

Aperçu rapide pour MMP2 anticorps (AA 193-545) (ABIN1886151)

Antigène: MMP2 (Matrix Metalloproteinase 2 (MMP2))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MMP2 est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (IF)

Détail du produit anti-MMP2 anticorps

Épitope: AA 193-545

Purification: Purified by antigen-affinity chromatography.

Immunogène: Recombinant protein fragment contain a sequence corresponding to a region within amino acids 193 and 545 of Human MMP2

Information d'application

Indications d'application: Suggested dilutions:
Western blotting: 1.500-1.3000
Immunofluorescence: 1.100-1.200

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: 0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

Agent conservateur: Thimerosal (Merthiolate)

Précaution d'utilisation: Biohazard Informations: This product contains thimerosal which is hazardous.

Stock: 4 °C/-20 °C

Stockage commentaire: Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.

Détails sur MMP2

Antigène: MMP2 (Matrix Metalloproteinase 2 (MMP2))

Autre désignation: MMP2

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.This gene encodes an enzyme which degrades type IV collagen, the major structural component of basement membranes.The enzyme plays a role in endometrial menstrual breakdown, regulation of vascularization and the inflammatory response.Mutations in this gene have been associated with Winchester syndrome and Nodulosis-Arthropathy-Osteolysis (NAO) syndrome.Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq]

Poids moléculaire: 74 kDa

ID gène: 4313

NCBI Accession: NM_004530, NP_004521

Pathways: Activation of Innate immune Response