MYH11 Rabbit Monoclonal Antibody

MYH11 Rabbit Monoclonal Antibody

Cat: AMRe83954
Boyut:50μL Fiyat:$168_x000D_
Boyut:100μL Fiyat:$300_x000D_
Uygulama:WB,IHC,ICC/IF,ICC
Reaktivite:Human
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:MYH11
Category: 組換えモノクローナル抗体 Tags: , , , , , , ,
MYH11 Rabbit Monoclonal Antibody
Konjugasyon: Unconjugated
Recombinant rabbit monoclonal antibody
Uygulama
IHC  ICC/IF  ELISA WB,IHC,ICC/IF,ICC
Reaktivite
Human
Gen Adı
MYH11
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı MYH11 Rabbit Monoclonal Antibody
Açıklama Recombinant rabbit monoclonal antibody
Konak Rabbit
Reaktivite Human
Konjugasyon Unconjugated
Modifikasyon Unmodified
İzotip IgG
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 PBS with 0.05% sodium azide,0.05% protective protein and 50% glycerol.
Saflaştırma Affinity Purification
Antijen Bilgisi
Gen Adı MYH11
Alternatif İsimler AAT4; FAA4; MYH11; Myosin 11; Myosin heavy chain 11; Myosin heavy chain smooth muscle isoform; Myosin heavy polypeptide 11 smooth muscle; SMHC; SMMHC;;Myosin heavy chain 11
Gen Kimliği -
SwissProt Kimliği P35749
İmmünojen A synthesized peptide derived from human Myosin heavy chain 11
Uygulama
Uygulama WB,IHC,ICC/IF,ICC
Seyreltme Oranı WB 1:1000-1:2000,IHC 1:100-1:200,ICC/IF 1:50-1:200,ICC 1:50-1:200
Moleküler Ağırlık 227 kDa
Araştırma Alanı
Arka Plan
The protein encoded by this gene is a smooth muscle myosin belonging to the myosin heavy chain family. The gene product is a subunit of a hexameric protein that consists of two heavy chain subunits and two pairs of non-identical light chain subunits. It functions as a major contractile protein, converting chemical energy into mechanical energy through the hydrolysis of ATP. A chromosomal rearrangement involving this gene is associated with acute myeloid leukemia of the M4Eo subtype. Mutations in this gene are associated with visceral myopathy, megacystis-microcolon-intestinal hypoperistalsis syndrome 2, and familial thoracic aortic aneurysm 4.
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