公司產(chǎn)品僅供科研研究實驗，不得用于臨床！
商品詳情：
英文名稱：MORN4/C10orf83
中文名稱：10號染色體開放閱讀框83抗體
別 名；44050 protein; C10orf83; Chromosome 10 open reading frame 83; MORN repeat containing 4; MORN repeat-containing protein 4; Morn4; MORN4_HUMAN; Protein 44050; Retinophilin.
研究領域；細胞生物 免疫學
抗體來源；Rabbit
克隆類型；Polyclonal
交叉反應； Mouse, (predicted: Human, Rat, Dog, Cow, Horse, )
產(chǎn)品應用；ELISA=1:5000-10000 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）
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量；16kDa
性 狀；Liquid
濃 度；1mg/ml
免 疫 原；KLH conjugated synthetic peptide derived from human MORN4/C10orf83: 101-146/146
亞 型；IgG
純化方法；affinity purified by Protein A
緩 沖 液；0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件；Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
注意事項；This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
產(chǎn)品介紹； MORN4 is a 146 amino acid protein that contains four MORN repeats and exists as two alternatively spliced isoforms. The gene encoding MORN4 maps to human chromosome 10, which contains over 800 genes and 135 million nucleotides, making up nearly 4.5% of the human genome. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. The chromosome 10 encoded gene ERCC6 is important for DNA repair and is linked to Cockayne syndrome which is characterized by extreme photosensitivity and premature aging. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10. As with most trisomies, trisomy 10 is rare and is deleterious.
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