Phospho-Nucleophosmin (Thr95) Rabbit Monoclonal Antibody

Phospho-Nucleophosmin (Thr95) Rabbit Monoclonal Antibody

Cat: AMRe87442
Boyut:50μL Fiyat:$168_x000D_
Boyut:100μL Fiyat:$300_x000D_
Uygulama:WB
Reaktivite:Human
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:Phospho-Nucleophosmin (Thr95)
Category: 組換えモノクローナル抗体 Tags: , , , ,
Phospho-Nucleophosmin (Thr95) Rabbit Monoclonal Antibody
Konjugasyon: Unconjugated
Recombinant rabbit monoclonal antibody
Uygulama
IHC  ICC/IF  ELISA WB
Reaktivite
Human
Gen Adı
Phospho-Nucleophosmin (Thr95)
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı Phospho-Nucleophosmin (Thr95) Rabbit Monoclonal Antibody
Açıklama Recombinant rabbit monoclonal antibody
Konak Rabbit
Reaktivite Human
Konjugasyon Unconjugated
Modifikasyon Phosphorylated
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 Phospho-Nucleophosmin (Thr95)
Alternatif İsimler B23; NPM
Gen Kimliği 4869
SwissProt Kimliği P06748
İmmünojen A synthetic phosphopeptide corresponding to residues surrounding Thr95 of human Nucleophosmin
Uygulama
Uygulama WB
Seyreltme Oranı WB 1:1000-1:5000
Moleküler Ağırlık Calculated MW:33 kDa; Observed MW:38 kDa
Araştırma Alanı
Arka Plan
The protein encoded by this gene is involved in several cellular processes, including centrosome duplication, protein chaperoning, and cell proliferation. The encoded phosphoprotein shuttles between the nucleolus, nucleus, and cytoplasm, chaperoning ribosomal proteins and core histones from the nucleus to the cytoplasm. This protein is also known to sequester the tumor suppressor ARF in the nucleolus, protecting it from degradation until it is needed. Mutations in this gene are associated with acute myeloid leukemia. Dozens of pseudogenes of this gene have been identified. [provided by RefSeq, Aug 2017]
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