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(zhì)量反饋  關于我們  聯(lián)系我們
亚洲人成电影在线天堂色,在线免费观看黄片欧美
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-Arginine vasopressin/HRP Conjugated antibody (bs-37002R-HRP)
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(chǎn)品編號 bs-37002R-HRP
英文名稱 Rabbit Anti-Arginine vasopressin/HRP Conjugated antibody
中文名稱 辣根過氧化物酶標記的抗利尿激素/血管升壓素/加壓素/血管加壓素抗體
別    名 Vasopressin; Antidiuretic Hormone; Arginine Vasopressin; ADH; Arginine vasopressin neurophysin II; ARVP; AVP; AVP NPII; AVRP; Vasopressin neurophysin 2 copeptin precursor; Vasopressin neurophysin II copeptin; VP; NEU2_HUMAN.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
產(chǎn)品類型 小分子抗體 
研究領域 心血管  細胞生物  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, )
產(chǎn)品應用 ELISA=1:100-1000 IHC-P=1:50-200 IHC-F=1:50-200 ICC=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 1.084kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated Arginine vasopressin
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 Constituents: 0.01M PBS, pH 7.4 with 10 mg/mL BSA and 0.1% Gentamicin, 50% glycerol. Or Lyophilized. Buffer = 0.01M PBS, pH 7.4 with 10 mg/mL BSA and 0.1% Gentamicin. Reconstitute with sterile distilled water.
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:
Vasopressin, also known as arginine vasopressin (AVP) or antidiuretic hormone (ADH), is a posterior pituitary hormone that is synthesised in the hypothalamus. Vasopressin is synthesised as a precursor protein that consists of arginine vasopressin and two associated proteins, neurophysin 2 and the glycopeptide copeptin. Vasopressin, together with its carrier protein neurophysin II, is packaged into neurosecretory vesicles and transported axonally to the nerve endings in the neurohypophysis, where it is either stored or secreted into the bloodstream. Vasopressin acts as a growth factor by enhancing pH regulation through acid-base transport systems. It has a direct antidiuretic action on the kidney and also causes vasoconstriction of the peripheral vessels. Vasopressin can also contract smooth muscle during parturition and lactation. It also plays a role in cognition, tolerance, adaptation and complex sexual and maternal behaviour, as well as in the regulation of water excretion and cardiovascular functions. Mutations in the vasopressin precursor cause autosomal dominant neurohypophyseal diabetes insipidus (ADNDI), which is characterised by persistant thirst, polydipsia and polyuria.

Function:
Neurophysin 2 specifically binds vasopressin.
Vasopressin has a direct antidiuretic action on the kidney, it also causes vasoconstriction of the peripheral vessels.

Subcellular Location:
Secreted.

DISEASE:
Defects in AVP are the cause of autosomal dominant neurohypophyseal diabetes insipidus (ADNDI) [MIM:125700]. ADNDI is characterized by persistent thirst, polydipsia and polyuria. The disease is transmitted in an autosomal dominant mode and appears to be largely if not completely penetrant.
Defects in AVP are the cause of autosomal recessive neurohypophyseal diabetes insipidus (ARNDI) [MIM:125700]. ARNDI is characterized by persistent thirst, polydipsia and polyuria. Most mutations are hypothesized to trigger neurodegeneration via disruption of preproAVP-NPII processing.

Similarity:
Belongs to the vasopressin/oxytocin family.

Database links:

Entrez Gene: 551 Human

Omim: 192340 Human

SwissProt: P01185 Human

Unigene: 89648 Human



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(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
欧美 亚洲 日本 国产| 久久精品国产亚洲高清| 留学生美女被大黑屌猛戳| 美国女人抠插bbb| 欧美日韩亚洲人人夜夜澡| 欧美综合区自拍亚洲综合| 久久精品一区二区三区免费看| 97超视频免费在线观看| 伊人久久综合无码成人网| 久久久精品日韩一区二区三区| 在线免费观看一区二区三区| 亚洲大尺度无码无码专线一区| 国产成人无码AV一区二区三区| 日本高清一区二区三区不卡| 99国产精品一区二区| ai换脸久久一区二区亚洲av| 制服丝袜国产在线第一页| 亚洲中文字幕在线无码一区二区| 骚逼被操视频拳交| 亚洲一区二区三成人精品| 胸大裸体美女视频| 欧美人与动人物A级| 国奴精品毛片av一区二区三区| 大鸡吧天天草黑逼| 大鸡吧干小逼逼视频大全| 狗狗大鸡巴狂操美女| 国产合区在线一区二区三区| 最新日本一区二区三区免费看| 黑人与日本人妻中文字幕| 亚洲另类激情在线观看| 亚洲一区二区三成人精品| 午夜精品在线视频| 亚洲欧美中文字幕第二十| 非洲人粗大长硬配种视频| 韩国女主播一区二区视频| 国产精品一区二区三区涩涩av| 人妻波多野结衣爽到喷水| 亚洲AV无码一区二区三区天堂古| 一区二区三区亚洲av| 中文字幕亚洲欧美精品一区二区| 美女麻豆颜色光屁股眼子|