MMP2 Mouse Monoclonal Antibody

MMP2 Mouse Monoclonal Antibody

Cat: AMM85917
Boyut:50μL Fiyat:$168_x000D_
Boyut:100μL Fiyat:$300_x000D_
Uygulama:WB,IHC,ICC
Reaktivite:Human
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:MMP2
Category: マウスモノクローナル抗体 Tags: , , , , , ,
MMP2 Mouse Monoclonal Antibody
Konjugasyon: Unconjugated
Mouse monoclonal Antibody
Uygulama
IHC  ICC/IF  ELISA WB,IHC,ICC
Reaktivite
Human
Gen Adı
MMP2
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı MMP2 Mouse Monoclonal Antibody
Açıklama Mouse monoclonal Antibody
Konak Mouse
Reaktivite Human
Konjugasyon Unconjugated
Modifikasyon Unmodified
İzotip Mouse IgG2b
Klonalite Monoclonal
Form Liquid
Konsantrasyon Unconjugated
Saklama Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Nakliye Ice bags.
Tampon Purified antibody in TBS with 0.05% sodium azide.
Saflaştırma Affinity Purification
Antijen Bilgisi
Gen Adı MMP2
Alternatif İsimler 72 kDa type IV collagenase, 72 kDa gelatinase, Gelatinase A, Matrix metalloproteinase-2, MMP-2, TBE-1, PEX, MMP2, CLG4A
Gen Kimliği 4313
SwissProt Kimliği P08253
İmmünojen This MMP2 monoclonal antibody is generated from mouse immunized with MMP2 recombinant protein.
Uygulama
Uygulama WB,IHC,ICC
Seyreltme Oranı WB 1:500-1:1000,IHC 1:100-1:500,ICC 1:20-1:50
Moleküler Ağırlık 73.9kDa
Araştırma Alanı
Arka Plan
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.
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