Perforin Rabbit Polyclonal Antibody

Perforin Rabbit Polyclonal Antibody

Cat: APRab00479
Boyut:20μL Fiyat:$99_x000D_
Boyut:50μL Fiyat:$150_x000D_
Boyut:100μL Fiyat:$280_x000D_
Boyut:200μL Fiyat:$520_x000D_
Uygulama:WB,IHC,ELISA
Reaktivite:Human
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:PRF1
Category: ポリクローナル抗体 Tags: , , , , , , ,
Perforin Rabbit Polyclonal Antibody
Konjugasyon: Unconjugated
Rabbit polyclonal Antibody
Uygulama
IHC  ICC/IF  ELISA WB,IHC,ELISA
Reaktivite
Human
Gen Adı
PRF1
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı Perforin Rabbit Polyclonal Antibody
Açıklama Rabbit polyclonal Antibody
Konak Rabbit
Reaktivite Human
Konjugasyon Unconjugated
Modifikasyon Unmodified
İzotip IgG
Klonalite Polyclonal
Form Liquid
Konsantrasyon Unconjugated
Saklama Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Nakliye Ice bags.
Tampon Liquid in PBS containing 50% glycerol, 0.5% protective protein and 0.02% sodium azide, pH 7.3.
Saflaştırma Affinity Purification
Antijen Bilgisi
Gen Adı PRF1
Alternatif İsimler Perforin-1; P1; Cytolysin; Lymphocyte pore-forming protein; PFP
Gen Kimliği 5551
SwissProt Kimliği P14222
İmmünojen The antiserum was produced against synthesized peptide derived from the C-terminal region of human PRF1. AA range:451-500
Uygulama
Uygulama WB,IHC,ELISA
Seyreltme Oranı WB 1:500-1:1000,IHC 1:50-1:100,ELISA 1:5000-1:20000
Moleküler Ağırlık Calculated MW: 61 kDa; Observed MW: 61 kDa
Araştırma Alanı
Immunology
Arka Plan
The protein encoded by this gene has structural and functional similarities to complement component 9 (C9). Like C9, this protein creates transmembrane tubules and is capable of lysing non-specifically a variety of target cells. This protein is one of the main cytolytic proteins of cytolytic granules, and it is known to be a key effector molecule for T-cell- and natural killer-cell-mediated cytolysis. Defects in this gene cause familial hemophagocytic lymphohistiocytosis type 2 (HPLH2), a rare and lethal autosomal recessive disorder of early childhood. Alternative splicing results in multiple transcript variants encoding the same protein.
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