RSK2 Rabbit Monoclonal Antibody

RSK2 Rabbit Monoclonal Antibody

Cat: AMRe03192
Beden:50μL Fiyat:$158 $99_x000D_
Beden:100μL Fiyat:$288 $180_x000D_
Uygulama:WB,IHC,IP
Reaktivite:Human,Hamster
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:RPS6KA3
Category: 組換えモノクローナル抗体 Tags: , , , , , , , ,
RSK2 Rabbit Monoclonal Antibody
Konjugasyon: Unconjugated
Recombinant rabbit monoclonal antibody
Uygulama
IHC  ICC/IF  ELISA WB,IHC,IP
Reaktivite
Human,Hamster
Gen Adı
RPS6KA3
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı RSK2 Rabbit Monoclonal Antibody
Açıklama Recombinant rabbit monoclonal antibody
Konak Rabbit
Reaktivite Human,Hamster
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 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% Sodium azide and 0.05% protective protein
Saflaştırma Affinity Purification
Antijen Bilgisi
Gen Adı RPS6KA3
Alternatif İsimler RPS6KA3; ISPK1; MAPKAPK1B; RSK2; Ribosomal protein S6 kinase alpha-3; S6K-alpha-3; 90 kDa ribosomal protein S6 kinase 3; p90-RSK 3; p90RSK3; Insulin-stimulated protein kinase 1; ISPK-1; MAP kinase-activated protein kinase 1b; MAPK-activated
Gen Kimliği 6197
SwissProt Kimliği P51812
İmmünojen A synthetic peptide corresponding to target protein
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: 84 kDa; Observed MW: 84 kDa
Araştırma Alanı
Signal Transduction
Arka Plan
This gene encodes a member of the RSK (ribosomal S6 kinase) family of serine/threonine kinases. This kinase contains 2 non-identical kinase catalytic domains and phosphorylates various substrates, including members of the mitogen-activated kinase (MAPK) signalling pathway. The activity of this protein has been implicated in controlling cell growth and differentiation. Mutations in this gene have been associated with Coffin-Lowry syndrome (CLS).
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