SULT2A1/ST2 Rabbit Monoclonal Antibody

SULT2A1/ST2 Rabbit Monoclonal Antibody

Cat: AMRe87157
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:SULT2A1/ST2
Category: 組換えモノクローナル抗体 Tags: , , , , , , , , ,
SULT2A1/ST2 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
SULT2A1/ST2
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı SULT2A1/ST2 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 SULT2A1/ST2
Alternatif İsimler HST; ST2; STD; hSTa; DHEAS; ST2A1; ST2A3; DHEA-ST
Gen Kimliği 6822
SwissProt Kimliği Q06520
İmmünojen A synthetic peptide of human SULT2A1/ST2
Uygulama
Uygulama WB,IHC,ICC/IF,FC
Seyreltme Oranı WB 1:1000-1:5000,IHC 1:500-1:2000,ICC/IF 1:20-1:50,FC 1:50-1:200
Moleküler Ağırlık Calculated MW:34 kDa; Observed MW:34 kDa
Araştırma Alanı
Arka Plan
This gene encodes a member of the sulfotransferase family. Sulfotransferases aid in the metabolism of drugs and endogenous compounds by converting these substances into more hydrophilic water-soluble sulfate conjugates that can be easily excreted. This protein catalyzes the sulfation of steroids and bile acids in the liver and adrenal glands, and may have a role in the inherited adrenal androgen excess in women with polycystic ovary syndrome. [provided by RefSeq, Mar 2010]
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