HIRA Rabbit Monoclonal Antibody

HIRA Rabbit Monoclonal Antibody

Cat: AMRe86418
Boyut:50μL Fiyat:$168_x000D_
Boyut:100μL Fiyat:$300_x000D_
Uygulama:WB,ICC/IF,FC,IP
Reaktivite:Human
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:HIRA
Category: 組換えモノクローナル抗体 Tags: , , , , , , ,
HIRA Rabbit Monoclonal Antibody
Konjugasyon: Unconjugated
Recombinant rabbit monoclonal antibody
Uygulama
IHC  ICC/IF  ELISA WB,ICC/IF,FC,IP
Reaktivite
Human
Gen Adı
HIRA
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı HIRA Rabbit Monoclonal Antibody
Açıklama Recombinant rabbit monoclonal antibody
Konak Rabbit
Reaktivite Human
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 HIRA
Alternatif İsimler TUP1; DGCR1; TUPLE1
Gen Kimliği 7290
SwissProt Kimliği P54198
İmmünojen A synthetic peptide of human HIRA
Uygulama
Uygulama WB,ICC/IF,FC,IP
Seyreltme Oranı WB 1:1000-1:5000,ICC/IF 1:50-1:200,FC 1:100-1:1000,IP 1:10-1:100
Moleküler Ağırlık Calculated MW:112 kDa; Observed MW:112 kDa
Araştırma Alanı
Arka Plan
This gene encodes a histone chaperone that preferentially places the variant histone H3.3 in nucleosomes. Orthologs of this gene in yeast, flies, and plants are necessary for the formation of transcriptionally silent heterochomatin. This gene plays an important role in the formation of the senescence-associated heterochromatin foci. These foci likely mediate the irreversible cell cycle changes that occur in senescent cells. It is considered the primary candidate gene in some haploinsufficiency syndromes such as DiGeorge syndrome, and insufficient production of the gene may disrupt normal embryonic development. [provided by RefSeq, Jul 2008]
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