亚洲中文字幕特级毛片-亚洲制服丝袜中文字幕-亚洲制服丝袜在线观看-亚洲制服欧美自拍另类-免费一级黄色-免费一级国产生活片

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
91成人免费在线视频,夫妇交换性三中文字幕,国产丫丫视频私人影院
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-HSD3B2/Biotin Conjugated antibody (bs-24205R-Bio)
訂購熱線:400-901-9800
訂購郵箱:sales@www.chomd.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@www.chomd.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-24205R-Bio
英文名稱1 Rabbit Anti-HSD3B2/Biotin Conjugated antibody
中文名稱 生物素標記的2型腎上腺皮質增生癥蛋白抗體
別    名 3 beta HSD adrenal and gonadal type; 3 beta HSD II; 3 beta HSD type II; 3 beta hydroxy 5 ene steroid dehydrogenase; 3 beta hydroxy Delta(5) steroid dehydrogenase; 3 beta hydroxysteroid dehydrogenase/Delta 5-->4-isomerase type 2; 3 beta-hydroxysteroid dehydrogenase type II, delta 5-delta 4-isomerase type II, 3 beta-HSD type II; 3 beta-hydroxysteroid dehydrogenase/Delta 5-->4-isomerase type II; 3 beta-hydroxysteroid dehydrogenase/Delta 5-->4-isomerase type 2; 3-beta-HSD II; 3-beta-hydroxy-5-ene steroid dehydrogenase; 3-beta-hydroxy-Delta(5)-steroid dehydrogenase; 3BHS2_HUMAN; ADRENAL HYPERPLASIA II; beta-hydroxysteroid dehydrogenase/Delta 5-->4-isomerase type 2; delta 5 delta 4 isomerase type II; Delta-5-3-ketosteroid isomerase; HSD3B; HSD3B2; HSDB; HSDB3B; hydroxy delta 5 steroid dehydrogenase, 3 beta and steroid delta isomerase 2; Hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2; Progesterone reductase.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 細胞生物  信號轉導  生長因子和激素  新陳代謝  線粒體  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Mouse, 
產品應用 WB=1:50-200 IHC-P=1:50-200 IHC-F=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 40kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from mouse HSD3B2
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:
3-beta-HSD is a bifunctional enzyme, that catalyzes the oxidative conversion of Delta(5)-ene-3-beta-hydroxy steroid, and the oxidative conversion of ketosteroids. The 3-beta-HSD enzymatic system plays a crucial role in the biosynthesis of all classes of hormonal steroids.

Function:
3-beta-HSD is a bifunctional enzyme, that catalyzes the oxidative conversion of Delta(5)-ene-3-beta-hydroxy steroid, and the oxidative conversion of ketosteroids. The 3-beta-HSD enzymatic system plays a crucial role in the biosynthesis of all classes of hormonal steroids.

Subunit:
Expressed in adrenal gland, testis and ovary.

Subcellular Location:
Endoplasmic reticulum membrane. Mitochondrion membrane.

Tissue Specificity:
Defects in HSD3B2 are the cause of adrenal hyperplasia type 2 (AH2) [MIM:201810]. AH2 is a form of congenital adrenal hyperplasia, a common recessive disease due to defective synthesis of cortisol. Congenital adrenal hyperplasia is characterized by androgen excess leading to ambiguous genitalia in affected females, rapid somatic growth during childhood in both sexes with premature closure of the epiphyses and short adult stature. Four clinical types: 'salt wasting' (SW, the most severe type), 'simple virilizing' (SV, less severely affected patients), with normal aldosterone biosynthesis, 'non-classic form' or late onset (NC or LOAH), and 'cryptic' (asymptomatic). In AH2, virilization is much less marked or does not occur. AH2 is frequently lethal in early life.
Note=Mild HSD3B2 deficiency in hyperandrogenic females is associated with characteristic traits of polycystic ovary syndrome, such as insulin resistance and luteinizing hormon hypersecretion.

DISEASE:
Defects in HSD3B2 are the cause of adrenal hyperplasia type 2 (AH2) [MIM:201810]. AH2 is a form of congenital adrenal hyperplasia, a common recessive disease due to defective synthesis of cortisol. Congenital adrenal hyperplasia is characterized by androgen excess leading to ambiguous genitalia in affected females, rapid somatic growth during childhood in both sexes with premature closure of the epiphyses and short adult stature. Four clinical types: 'salt wasting' (SW, the most severe type), 'simple virilizing' (SV, less severely affected patients), with normal aldosterone biosynthesis, 'non-classic form' or late onset (NC or LOAH), and 'cryptic' (asymptomatic). In AH2, virilization is much less marked or does not occur. AH2 is frequently lethal in early life.
Note=Mild HSD3B2 deficiency in hyperandrogenic females is associated with characteristic traits of polycystic ovary syndrome, such as insulin resistance and luteinizing hormon hypersecretion

Similarity:
Belongs to the 3-beta-HSD family.

Database links:

Entrez Gene: 3283 Huma

Entrez Gene: 3284 Human

Entrez Gene: 15492 Mouse

Entrez Gene: 15493 Mouse

Entrez Gene: 15494 Mouse

Entrez Gene: 29632 Rat

Entrez Gene: 360348 Rat

Entrez Gene: 682974 Rat

Omim: 201810 Human

SwissProt: P14060 Human

SwissProt: P26439 Human

SwissProt: O35469 Mouse

SwissProt: P24815 Mouse

SwissProt: P26149 Mouse

SwissProt: P26150 Mouse

SwissProt: P22071 Rat

SwissProt: P22072 Rat

SwissProt: Q62878 Rat

Unigene: 364941 Human

Unigene: 654399 Human

Unigene: 140811 Mouse

Unigene: 14435 Mouse

Unigene: 158717 Mouse

Unigene: 482364 Mouse

Unigene: 109394 Rat

Unigene: 128814 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.www.chomd.com.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
主站蜘蛛池模板: 亚洲无人影院av| 日韩一区二区超清视频在线 | 91香蕉蜜桃草莓榴莲秋葵18禁| 无限资源视频手机在线观看免费 | 91在线无码精品秘?入口91| 亚洲人影院在线观看未满十八岁的时候 | 嗯啊开小嫩苞好深啊h日本视频许先生 | 日韩内射美女片在线观看网站| 狠狠色丁香婷婷综合尤物.狠狠色噜噜狠狠狠777米奇小说 | 亚洲第一极品精品无码久久,精品国产一 | 亚洲精品久久久一区二区三区 | 亚洲级女?片www777自述| 精品无码视频在线观看下载免费| 97夜夜澡人人爽人人?| 午夜伦伦电影理论片2022 在线观看| 久久精品国内一区二区三区卡通无码 | 四虎牲无码www,1515 - com | 2019天堂精品视频在线观看免费| 丝袜美腿三区=区一区| 国产精品亚洲AV三区黑牛牛影视 | 成人网站在线观看尤物网站| 亚洲AV色香蕉一区二区三区老师 | 日本伊人精品一区二区三区观看方式| 国产无遮挡成人免费视频网站游戏 | 一级A片印度女人高潮| 久久综合九色综合久99-日韩精品无码 | 久久精品青草社区特色 | 99999久久久久久亚洲一本道 | 国产自在自钱2| 极品腹肌军警男自慰XNXX | 日韩三级在线观看视频.欧美精品日韩 | 96精品无码国产在线观看一区 | 日韩精品一区二三区中文-亚洲高清偷拍一区二区三区 | 精品国产一区二区三区无码-亚洲一区| 中文字幕无码综合视频网站| 一级视频免费观看APP| 精品一区二区三区在线成人3d动漫 | gogogo免费观看国语一区二区| 中文字幕岛国片麻豆视频| 久久夜色撩人精品国产APP免费| 综合无码一区二区三区色欲|