TGFB2 Mouse Monoclonal Antibody

TGFB2 Mouse Monoclonal Antibody

Cat: AMM86048
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:TGFB2
Category: マウスモノクローナル抗体 Tags: , , , , , , , ,
TGFB2 Mouse Monoclonal Antibody
Konjugasyon: Unconjugated
Mouse monoclonal Antibody
Uygulama
IHC  ICC/IF  ELISA WB,IHC,ICC
Reaktivite
Human
Gen Adı
TGFB2
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı TGFB2 Mouse Monoclonal Antibody
Açıklama Mouse monoclonal Antibody
Konak Mouse
Reaktivite Human
Konjugasyon Unconjugated
Modifikasyon Unmodified
İzotip Mouse IgG1
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 TGFB2
Alternatif İsimler Transforming growth factor beta-2, TGF-beta-2, BSC-1 cell growth inhibitor, Cetermin, Glioblastoma-derived T-cell suppressor factor, G-TSF, Polyergin, Latency-associated peptide, LAP, TGFB2
Gen Kimliği 7042
SwissProt Kimliği P61812
İmmünojen This TGFB2 monoclonal antibody is generated from mouse immunized with TGFB2 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 47.7kDa
Araştırma Alanı
TGF-beta signaling pathway,MAPK signaling pathway
Arka Plan
This gene encodes a member of the transforming growthfactor beta (TGFB) family of cytokines, which are multifunctionalpeptides that regulate proliferation, differentiation, adhesion,migration, and other functions in many cell types by transducingtheir signal through combinations of transmembrane type I and typeII receptors (TGFBR1 and TGFBR2) and their downstream effectors,the SMAD proteins. Disruption of the TGFB/SMAD pathway has beenimplicated in a variety of human cancers. The encoded protein issecreted and has suppressive effects of interleukin-2 dependentT-cell growth. Translocation t(1;7)(q41;p21) between this gene andHDAC9 is associated with Peters' anomaly, a congenital defect ofthe anterior chamber of the eye. The knockout mice lacking thisgene show perinatal mortality and a wide range of developmental,including cardiac, defects. Alternatively spliced transcriptvariants encoding different isoforms have been identified.
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