MYH9 Rabbit Monoclonal antibody

MYH9 Rabbit Monoclonal antibody

Cat: AMRe03116
Beden:50μL Fiyat:$168 $99_x000D_
Beden:100μL Fiyat:$300 $180_x000D_
Uygulama:WB,IHC,IP
Reaktivite:Human,Rat
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:MYH9
Category: 組換えモノクローナル抗体 Tags: , , , , , , , ,
MYH9 Rabbit Monoclonal antibody
Konjugasyon: Unconjugated
Recombinant rabbit monoclonal antibody
Uygulama
IHC  ICC/IF  ELISA WB,IHC,IP
Reaktivite
Human,Rat
Gen Adı
MYH9
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı MYH9 Rabbit Monoclonal antibody
Açıklama Recombinant rabbit monoclonal antibody
Konak Rabbit
Reaktivite Human,Rat
Konjugasyon Unconjugated
Modifikasyon Unmodified
İzotip IgG
Klonalite Monoclonal Antibody
Form Liquid
Konsantrasyon Unconjugated
Saklama Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Nakliye Ice bags.
Tampon 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% Sodium azide and 0.05% protective protein
Saflaştırma Affinity Purified
Antijen Bilgisi
Gen Adı MYH9
Alternatif İsimler MHA; FTNS; EPSTS; BDPLT6; DFNA17; MATINS; NMMHCA; NMHC-II-A; NMMHC-IIA
Gen Kimliği 4627
SwissProt Kimliği P35579
İmmünojen A synthetic peptide of human non-muscle Myosin IIA
Uygulama
Uygulama WB,IHC,IP
Seyreltme Oranı WB 1:500-1:1000,IHC 1:50-1:100,IP 1:20-1:50
Moleküler Ağırlık Calculated MW: 227 kDa; Observed MW: 227 kDa
Araştırma Alanı
Signal Transduction
Arka Plan
This gene encodes a conventional non-muscle myosin; this protein should not be confused with the unconventional myosin-9a or 9b (MYO9A or MYO9B). The encoded protein is a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain which is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in this gene have been associated with non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness. [provided by RefSeq, Dec 2011]
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