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一抗(kàng)
英文(wén)名(míng)稱 Anti-C5ORF42
中文名(míng)稱 5號染色體開(kāi)放(fàng)閱讀框(kuàng)42抗體
別(bié) 名 Chromosome 5 open reading frame 42; FLJ13231; Hypothetical protein LOC65250; Transmembrane protein ENSP; Uncharacterized protein C5orf42; CE042_HUMAN.
詳(xiáng)細介紹：
濃 度 1mg/1ml
規(guī) 格 0.2ml/200μg
抗體來源 Rabbit
克隆(lóng)類(lèi)型(xíng) polyclonal
交(jiāo)叉反應(yīng) Human, Mouse, Rat, Dog, Cow, Sheep
產(chǎn)品類型(xíng) 一抗
研究領域(yù) 細胞生物 免疫(yì)學(xué)
蛋(dàn)白(bái)分(fēn)子(zǐ)量 predicted molecular weight: 362kDa
性(xìng) 狀 Lyophilized or Liquid
免 疫 原 KLH conjugated synthetic peptide derived from human C5ORF42
亞(yà) 型 IgG
純(chún)化(huà)方法 affinity purified by Protein A
儲 存 液(yè) Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4
產(chǎn)品應(yīng)用(yòng) WB=1:100-500 ELISA=1:500-1000 IP=1:20-100 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500
（石(shí)蠟(là)切(qiē)片需做抗(kàng)原修復(fù)）
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
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.
Important Note This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
相(xiāng)關資料：
產(chǎn)品(pǐn)介紹
Subcellular Location : Membrane; Multi-pass membrane protein (Potential).
DISEASE : Defects in C5orf42 are the cause of Joubert syndrome type 17 (JBTS17) [MIM:614615]. A disorder presenting with cerebellar ataxia, oculomotor apraxia, hypotonia, neonatal breathing abnormalities and psychomotor delay. Neuroradiologically, it is characterized by cerebellar vermian hypoplasia/aplasia, thickened and reoriented superior cerebellar peduncles, and an abnormally large interpeduncular fossa, giving the appearance of a molar tooth on transaxial slices (molar tooth sign). Additional variable features include retinal dystrophy and renal disease.
Database links : UniProtKB/Swiss-Prot: Q9H799.4
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