mm1313亚洲精品,欧美俄罗斯40老熟妇,欧美日韩在线观看视频在线,亚洲欧美国产激情综合在线

掃碼關注公眾號           掃碼咨詢技術支持           掃碼咨詢技術服務
  
客服熱線:400-901-9800  客服QQ:4009019800  技術答疑  技術支持  質量反饋  人才招聘  關于我們  聯系我們
久久精品亚洲乱码伦伦中文,国产av一区二区亚洲
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-CYP11B2/Cy3 Conjugated antibody (bs-10161R-Cy3)
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-10161R-Cy3
英文名稱1 Rabbit Anti-CYP11B2/Cy3 Conjugated antibody
中文名稱 Cy3標記的醛固酮合成酶CYP11B2抗體
別    名 CYP 11B2; CYPXI11B2; Cytochrome P450 1111B2; Cytochrome P450 1111B2 mitochondrial; Cytochrome P450 family 11 subfamily B polypeptide 2; Cytochrome P450 subfamily XIB (cholesterol side chain cleavage); Cytochrome P450 subfamily XI11B2; Cytochrome P450C1111B2; C11B2_HUMAN.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 心血管  細胞生物  免疫學  線粒體  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human,  (predicted: Mouse, Rat, Rabbit, )
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 58kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human CYP11B2
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.
產品介紹 background:
This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localizes to the mitochondrial inner membrane. The enzyme has steroid 18-hydroxylase activity to synthesize aldosterone and 18-oxocortisol as well as steroid 11 beta-hydroxylase activity. Mutations in this gene cause corticosterone methyl oxidase deficiency. [provided by RefSeq, Jul 2008].

Function:
Preferentially catalyzes the conversion of 11-deoxycorticosterone to aldosterone via corticosterone and 18-hydroxycorticosterone.

Subcellular Location:
Mitochondrion membrane.

DISEASE:
Defects in CYP11B2 are the cause of corticosterone methyloxidase type 1 deficiency (CMO-1 deficiency) [MIM:203400]; also known as aldosterone deficiency due to defect in 18-hydroxylase or aldosterone deficiency I. CMO-1 deficiency is an autosomal recessive disorder of aldosterone biosynthesis. There are two biochemically different forms of selective aldosterone deficiency be termed corticosterone methyloxidase (CMO) deficiency type 1 and type 2. In CMO-1 deficiency, aldosterone is undetectable in plasma, while its immediate precursor, 18-hydroxycorticosterone, is low or normal.
Defects in CYP11B2 are the cause of corticosterone methyloxidase type 2 deficiency (CMO-2 deficiency) [MIM:610600]. CMO-2 is an autosomal recessive disorder of aldosterone biosynthesis. In CMO-2 deficiency, aldosterone can be low or normal, but at the expense of increased secretion of 18-hydroxycorticosterone. Consequently, patients have a greatly increased ratio of 18-hydroxycorticosterone to aldosterone and a low ratio of corticosterone to 18-hydroxycorticosterone in serum.
Defects in CYP11B2 are a cause of familial hyperaldosteronism type 1 (FH1) [MIM:103900]. It is a disorder characterized by hypertension, variable hyperaldosteronism, and abnormal adrenal steroid production, including 18-oxocortisol and 18-hydroxycortisol. There is significant phenotypic heterogeneity, and some individuals never develop hypertension. Note=The molecular defect causing hyperaldosteronism familial type 1 is an anti-Lepore-type fusion of the CYP11B1 and CYP11B2 genes. The hybrid gene has the promoting part of CYP11B1, ACTH-sensitive, and the coding part of CYP11B2.

Similarity:
Belongs to the cytochrome P450 family.

Database links:

Entrez Gene: 1585 Human

Entrez Gene: 13072 Mouse

Entrez Gene: 24294 Rat

Omim: 124080 Human

SwissProt: P19099 Human

SwissProt: P15539 Mouse

SwissProt: P30099 Rat

Unigene: 632054 Human

Unigene: 377079 Mouse

Unigene: 144549 Rat



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權所有 2004-2026 www.m.p2b3.cn 北京博奧森生物技術有限公司
通過國際質量管理體系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         京公網安備110107000727號
97国产精品国偷自产在线| 亚洲高潮久久久久久| 国产亚洲视频中文字幕97精品| 学生妹在线观看无码| 中文字幕日韩欧美推理片免费观看| 国产亚洲黄色在线影院| 国产亚洲视频中文字幕97精品| 免费看中文字幕一级高清| 欧美亚洲综合中文字幕蜜桃成熟| 久久久1区2区3区| 久久精品水蜜挑AV综合天堂| 国产无遮挡又污又黄又爽| 精品无码中文字幕在线| 国产欧美精品区一区二区三区竹菊| 日韩欧美精品在线中文字幕| 午夜精品人妻一区二区三区| 欧美日韩一区二区中文字幕| 久久99精品免费免费| 亚洲精品在线观看日本国产| 久久婷婷综合激情亚洲狠狠| 欧美日本大陆一区二区| 亚洲欧美成人久久一区二区三区| 欧美一级大片免费观看视频| 93国产精品久久久久久| 国产精品va在线观看老妇女| 国产精品综合久久久久久| 精品国产尤物久久久久久| 欧美日韩国产成人精品自拍视频| 久久精品成人免费国产| 日本午夜福利在线视频| 亚洲精品夜夜夜妓女网| 国产精品18禁久久久久久久久| 日韩码一码二码三码区别| 亚洲成人蜜桃动漫一区| 日韩亚洲欧美综合在线| 亚洲欧美另类久久久精品| 亚洲欧美成人激情在线| 亚洲另类欧美在线中文字幕不卡| 免费在线观看一本视频| 亚洲国产精品一区二区三区久久| 夫妻久久久久久久久了|