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        Rabbit Anti-StAR/BF594 Conjugated antibody (bs-20387R-BF594)
        訂購熱線:400-901-9800
        訂購郵箱:sales@m.p2b3.cn
        訂購QQ:  400-901-9800
        技術支持:techsupport@m.p2b3.cn
        說 明 書: 100ul  
        100ul/2980.00元
        大包裝/詢價
        產品編號 bs-20387R-BF594
        英文名稱 Rabbit Anti-StAR/BF594 Conjugated antibody
        中文名稱 BF594標記的促黃體激素誘導蛋白抗體
        別    名 StARD1; Cholesterol trafficker; Luteinizing hormone induced protein; Mitochondrial steroid acute regulatory protein; StAR related lipid transfer (START) domain containing 1; StARD1; START domain containing protein 1; Steroidogenic Acute Regulatory Protein; Steroidogenic acute regulatory protein mitochondrial; STAR_HUMAN.  
        規(guī)格價格 100ul/2980元 購買        大包裝/詢價
        說 明 書 100ul  
        研究領域 腫瘤  免疫學  轉錄調節(jié)因子  激酶和磷酸酶  線粒體  
        抗體來源 Rabbit
        克隆類型 Polyclonal
        交叉反應 Human,  (predicted: Mouse, Rat, Pig, Horse, )
        產品應用 ICC=1:50-200 IF=1:50-200 
        not yet tested in other applications.
        optimal dilutions/concentrations should be determined by the end user.
        分 子 量 32kDa
        性    狀 Lyophilized or Liquid
        濃    度 1mg/ml
        免 疫 原 KLH conjugated synthetic peptide derived from human StAR
        亞    型 IgG
        純化方法 affinity purified by Protein A
        儲 存 液 Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4.
        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.
        產品介紹 background:
        The protein encoded by this gene plays a key role in the acute regulation of steroid hormone synthesis by enhancing the conversion of cholesterol into pregnenolone. This protein permits the cleavage of cholesterol into pregnenolone by mediating the transport of cholesterol from the outer mitochondrial membrane to the inner mitochondrial membrane. Mutations in this gene are a cause of congenital lipoid adrenal hyperplasia (CLAH), also called lipoid CAH. A pseudogene of this gene is located on chromosome 13. [provided by RefSeq, Jul 2008].

        Function:
        Plays a key role in steroid hormone synthesis by enhancing the metabolism of cholesterol into pregnenolone. Mediates the transfer of cholesterol from the outer mitochondrial membrane to the inner mitochondrial membrane where it is cleaved to pregnenolone.

        Subunit:
        May interact with TSPO.

        Subcellular Location:
        Mitochondrion.

        DISEASE:
        Defects in STAR are the cause of adrenal hyperplasia type 1 (AH1) [MIM:201710]. The most severe form of adrenal hyperplasia. It is a condition characterized by onset of profound adrenocortical insufficiency shortly after birth, hyperpigmentation reflecting increased production of pro-opiomelanocortin, elevated plasma rennin activity as a consequence of reduced aldosterone synthesis, and male pseudohermaphroditism resulting from deficient fetal testicular testosterone synthesis. Affected individuals are phenotypic females irrespective of gonadal sex, and frequently die in infancy if mineralocorticoid and glucocorticoid replacement are not instituted.

        Similarity:
        Contains 1 START domain.

        Database links:

        Entrez Gene: 6770 Human

        Entrez Gene: 20845 Mouse

        Entrez Gene: 25557 Rat

        Omim: 600617 Human

        SwissProt: P49675 Human

        SwissProt: P51557 Mouse

        SwissProt: P97826 Rat

        Unigene: 521535 Human

        Unigene: 293314 Mouse

        Unigene: 11399 Rat



        Important Note:
        This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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