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尿調(diào)節(jié)蛋白抗體

參   考   價: 80

訂  貨  量: ≥1 

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產(chǎn)品型號

品       牌Abcam

廠商性質(zhì)生產(chǎn)商

所  在  地上海

更新時間:2015-06-08 13:30:27瀏覽次數(shù):219次

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尿調(diào)節(jié)蛋白抗體
WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (石蠟切片需做抗原修復(fù))
not yet tested in other applications.

尿調(diào)節(jié)蛋白抗體

英文名稱 Uromucoid
中文名稱 尿調(diào)節(jié)蛋白抗體
別    名 Uromodulin; ADMCKD2; FJHN; HNFJ; HNFJ1; MCKD2; MGC14034; TAMM-HORSFALL; THGP; THP; UMOD; urehr4; Uromodulin; uromucoid; UROM_MOUSE; UROM_HUMAN.
 
說 明 書 0.1ml  
研究領(lǐng)域 細胞生物  
抗體來源 Mouse
克隆類型 Monoclonal
克 隆 號 2A9
交叉反應(yīng) Human, Mouse, Rat, Cow, 
產(chǎn)品應(yīng)用 WB=1:100-500 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (石蠟切片需做抗原修復(fù)) 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 68kDa
細胞定位 細胞膜 
性    狀 Lyophilized or Liquid
濃    度 1mg/1ml
免 疫 原 KLH conjugated synthetic peptide derived from human Uromucoid
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.

PubMed PubMed
產(chǎn)品介紹 background:
This gene encodes uromodulin, the most abundant protein in normal urine. 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. Uromodulin may act as a constitutive inhibitor of calcium crystallization in renal fluids. Excretion of uromodulin in urine may provide defense against urinary tract infections caused by uropathogenic bacteria. Defects in this gene are associated with the autosomal dominant renal disorders medullary cystic kidney disease-2 (MCKD2) and familial juvenile hyperuricemic nephropathy (FJHN). These disorders are characterized by juvenile onset of hyperuricemia, gout, and progressive renal failure. While several transcript variants may exist for this gene, the full-length natures of only two have been described to date. These two represent the major variants of this gene and encode the same isoform. [provided by RefSeq]
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xy-0486R    Integrin beta 1整合素β1/Integrin β1抗體
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