来一水AV@lysav|亚洲AV无码片VR一区二区三区 |国产亚洲精久久久久久无码|视色4se成人午夜精品久久

掃碼關(guān)注公眾號           掃碼咨詢技術(shù)支持           掃碼咨詢技術(shù)服務(wù)
  
客服熱線:400-901-9800  客服QQ:4009019800  技術(shù)答疑  技術(shù)支持  質(zhì)量反饋  人才招聘  關(guān)于我們  聯(lián)系我們
色ww色色ww色色|麻豆妓女爽爽一区二区三|国产精品婷婷一区二区
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-StAR/PE-Cy5.5 Conjugated antibody (bs-20388R-PE-Cy5.5)
訂購熱線:400-901-9800
訂購郵箱:sales@73327.net
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@73327.net
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-20388R-PE-Cy5.5
英文名稱1 Rabbit Anti-StAR/PE-Cy5.5 Conjugated antibody
中文名稱 PE-Cy5.5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(lǐng)域 腫瘤  免疫學  轉(zhuǎn)錄調(diào)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 Mouse, Rat,  (predicted: Human, Chicken, Dog, Pig, Cow, Horse, Rabbit, Sheep, )
產(chǎn)品應用 Flow-Cyt=1:50-200 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 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.
產(chǎn)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.
版權(quán)所有 2004-2026 www.73327.net 北京博奧森生物技術(shù)有限公司
通過國際質(zhì)量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號: 00124Q34771R2M/1100
通過國際醫(yī)療器械-質(zhì)量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號: CQC24QY10047R0M/1100
京ICP備05066980號-1         京公網(wǎng)安備110107000727號
天堂А√在线中文在线| 中文字幕AV一区二区三区| 一区二区国产欧美日韩无| 男人添女人囗交做爰视频| 全部免费毛片在线播放| 久久久久久综合岛国免费观看| 一本大道无码人妻精品专区| 国产精品普通话对白在线视频| 无码精品一区二区三区| 啊灬啊灬啊灬快灬高潮了| 亚洲AV永久无码精品一百度影院| 国产日韩久久久久久| 少妇高潮惨叫久久久久久| 亚洲女初尝黑人巨高清| 亚洲AV午夜精品一区二区三区 | 天天做夜夜躁狠狠躁视频| 熟睡人妻被讨厌的公侵犯| 成人午夜福利啊啊啊| 一本清日本在线视频精品| 黑人巨大JEEP日本人| 免费视频网站| 狠狠色综合网站久久久久久久| 乳尖乱颤娇喘连连A片在线观看 | 日韩人妻中文无码一区二区| 欧美成人色九九九色视| 又大又粗的免费视频| 日本韩国偷拍视频对白不卡高清精品| 国产精品人成视频免费播放| 久久免费看少妇高潮A片| 色婷婷av一区二区三区| 精品无码一区二区三区爱欲 | 99久久久国产精品45分钟| 亚洲综合精品天堂夜夜| 伊人WWW22综合色| 免费观看电视剧全集在线播放| 亚洲欧美日韩高清在线一区| AV无码一区二区乱子伦| 国产偷伦视频片免费观看图片 | 国产A级三级三级三级| 免费A级毛片在线播放不收费| 亚洲AV永久无码精品国产精品 |