Acetyl-p53 (Lys305) Rabbit Monoclonal Antibody

Acetyl-p53 (Lys305) Rabbit Monoclonal Antibody

Cat: AMRe87685
Boyut:50μL Fiyat:$168_x000D_
Boyut:100μL Fiyat:$300_x000D_
Uygulama:WB
Reaktivite:Human,Mouse,Rat
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:Acetyl-p53 (Lys305)
Category: 組換えモノクローナル抗体 Tags: , , , , , ,
Acetyl-p53 (Lys305) Rabbit Monoclonal Antibody
Konjugasyon: Unconjugated
Recombinant rabbit monoclonal antibody
Uygulama
IHC  ICC/IF  ELISA WB
Reaktivite
Human,Mouse,Rat
Gen Adı
Acetyl-p53 (Lys305)
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı Acetyl-p53 (Lys305) Rabbit Monoclonal Antibody
Açıklama Recombinant rabbit monoclonal antibody
Konak Rabbit
Reaktivite Human,Mouse,Rat
Konjugasyon Unconjugated
Modifikasyon Acetylated
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 Acetyl-p53 (Lys305)
Alternatif İsimler P53; BCC7; LFS1; TRP53
Gen Kimliği 7157, 22059, 24842
SwissProt Kimliği P04637, P02340, P10361
İmmünojen A synthetic acetylpeptide corresponding to residues surrounding Lys305 of human p53
Uygulama
Uygulama WB
Seyreltme Oranı WB 1:1000-1:5000
Moleküler Ağırlık Calculated MW:44 kDa; Observed MW:53 kDa
Araştırma Alanı
Arka Plan
This gene encodes a tumor suppressor protein containing transcriptional activation, DNA binding, and oligomerization domains. The encoded protein responds to diverse cellular stresses to regulate expression of target genes, thereby inducing cell cycle arrest, apoptosis, senescence, DNA repair, or changes in metabolism. Mutations in this gene are associated with a variety of human cancers, including hereditary cancers such as Li-Fraumeni syndrome. Alternative splicing of this gene and the use of alternate promoters result in multiple transcript variants and isoforms. Additional isoforms have also been shown to result from the use of alternate translation initiation codons from identical transcript variants (PMIDs: 12032546, 20937277). [provided by RefSeq, Dec 2016]
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