SERCA2 ATPase Rabbit Monoclonal Antibody

SERCA2 ATPase Rabbit Monoclonal Antibody

Cat: AMRe86415
Boyut:50μL Fiyat:$168_x000D_
Boyut:100μL Fiyat:$300_x000D_
Uygulama:WB,IHC,ICC/IF,FC
Reaktivite:Human,Mouse,Rat
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:SERCA2 ATPase
Category: 組換えモノクローナル抗体 Tags: , , , , , , , , ,
SERCA2 ATPase Rabbit Monoclonal Antibody
Konjugasyon: Unconjugated
Recombinant rabbit monoclonal antibody
Uygulama
IHC  ICC/IF  ELISA WB,IHC,ICC/IF,FC
Reaktivite
Human,Mouse,Rat
Gen Adı
SERCA2 ATPase
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı SERCA2 ATPase Rabbit Monoclonal Antibody
Açıklama Recombinant rabbit monoclonal antibody
Konak Rabbit
Reaktivite Human,Mouse,Rat
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 Supplied in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% protective protein. Stable for 12 months from date of receipt.
Saflaştırma Affinity Purification
Antijen Bilgisi
Gen Adı SERCA2 ATPase
Alternatif İsimler DD; DAR; ATP2B; SERCA2
Gen Kimliği 488
SwissProt Kimliği P16615
İmmünojen A synthetic peptide of human SERCA2 ATPase
Uygulama
Uygulama WB,IHC,ICC/IF,FC
Seyreltme Oranı WB 1:1000-1:5000,IHC 1:100-1:200,ICC/IF 1:200-1:500,FC 1:10-1:100
Moleküler Ağırlık Calculated MW:115 kDa; Observed MW:115 kDa
Araştırma Alanı
Arka Plan
This gene encodes one of the SERCA Ca(2+)-ATPases, which are intracellular pumps located in the sarcoplasmic or endoplasmic reticula of the skeletal muscle. This enzyme catalyzes the hydrolysis of ATP coupled with the translocation of calcium from the cytosol into the sarcoplasmic reticulum lumen, and is involved in regulation of the contraction/relaxation cycle. Mutations in this gene cause Darier-White disease, also known as keratosis follicularis, an autosomal dominant skin disorder characterized by loss of adhesion between epidermal cells and abnormal keratinization. Other types of mutations in this gene have been associated with various forms of muscular dystrophies. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2019]
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