Uromucoid Rabbit Monoclonal Antibody

Uromucoid Rabbit Monoclonal Antibody

Cat: AMRe86783
Boyut:50μL Fiyat:$168_x000D_
Boyut:100μL Fiyat:$300_x000D_
Uygulama:WB,IHC
Reaktivite:Human
Konjuge:Unconjugated
İsteğe bağlı konjugeler: Biotin, FITC (ücretsiz). Diğer 26 konjugatı görün.

Gen Adı:Uromucoid
Category: 組換えモノクローナル抗体 Tags: , , , , ,
Uromucoid Rabbit Monoclonal Antibody
Konjugasyon: Unconjugated
Recombinant rabbit monoclonal antibody
Uygulama
IHC  ICC/IF  ELISA WB,IHC
Reaktivite
Human
Gen Adı
Uromucoid
Saklama
Aliquot and store at -20°C (valid for 12 months). Avoid freeze/thaw cycles.
Özet
Ürün Adı Uromucoid 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 Uromucoid
Alternatif İsimler THP; FJHN; HNFJ; THGP; HNFJ1; MCKD2; ADMCKD2
Gen Kimliği 7369
SwissProt Kimliği P07911
İmmünojen Recombinant protein of human Uromucoid
Uygulama
Uygulama WB,IHC
Seyreltme Oranı WB 1:500-1:2000,IHC 1:500-1:2000
Moleküler Ağırlık Calculated MW:70 kDa; Observed MW:115 kDa
Araştırma Alanı
Arka Plan
The protein encoded by this gene is the most abundant protein in mammalian urine under physiological conditions. Its excretion in urine follows proteolytic cleavage of the ectodomain of its glycosyl phosphatidylinosital-anchored counterpart that is situated on the luminal cell surface of the loop of Henle. This protein may act as a constitutive inhibitor of calcium crystallization in renal fluids. Excretion of this protein in urine may provide defense against urinary tract infections caused by uropathogenic bacteria. Defects in this gene are associated with the renal disorders medullary cystic kidney disease-2 (MCKD2), glomerulocystic kidney disease with hyperuricemia and isosthenuria (GCKDHI), and familial juvenile hyperuricemic nephropathy (FJHN). Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2013]
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