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
国产无套中出学生姝,jizzjizz日本护士,全部免费a级毛片
首頁 > 產品中心 > 標記一抗 > 產品信息
Mouse Anti-Insulin (1G11)/Cy3 Conjugated antibody (bsm-0855M-Cy3)
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 bsm-0855M-Cy3
英文名稱1 Mouse Anti-Insulin (1G11)/Cy3 Conjugated antibody
中文名稱 Cy3標記的胰島素單克隆抗體
別    名 ILPR; INS; Insulin A chain; Insulin B chain; Insulin A chain; Insulin precursor; IRDN; Proinsulin; Proinsulin precursor; IDDM2; INS_HUMAN; MODY10.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 腫瘤  心血管  細胞生物  神經生物學  信號轉導  生長因子和激素  糖尿病  內分泌病  新陳代謝  
抗體來源 Mouse
克隆類型 Monoclonal
克 隆 號 1G11
交叉反應 (predicted: Human, )
產品應用
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 5.8/12kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 Recombinded human Insulin protein
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:
Insulin is a pancreatic hormone that regulates glucose and is involved in the synthesis of protein and fat. It increases cell permeability to monosaccharides, amino acids and fatty acids. It accelerates glycolysis, the pentose phosphate cycle, and glycogen synthesis in liver. Heterodimer of a B chain and an A chain linked by two disulfide bonds.Belongs to the insulin family. The insulin-link growth factors, IGF-I and IGF-II (also desinated somatomedin C and multiplication stimulating activator, respectvely), share approximatly 76% sequence identity and are 50% related to pro-insulin.IGF-I and IGF-II are nonglycosylated, single chain proteins of 70 and 76 amino acids in length, respectivelly. IGF-I functions as an autocrine regulator of growth in vaious, whereas the function of IGF-II is less well defined.

Function:
Insulin decreases blood glucose concentration. It increases cell permeability to monosaccharides, amino acids and fatty acids. It accelerates glycolysis, the pentose phosphate cycle, and glycogen synthesis in liver.

Subunit:
Heterodimer of a B chain and an A chain linked by two disulfide bonds.

Subcellular Location:
Secreted.

DISEASE:
Hyperproinsulinemia, familial (FHPRI) [MIM:176730]: An autosomal dominant condition characterized by elevated levels of serum proinsulin-like material. Note=The disease is caused by mutations affecting the gene represented in this entry.
Diabetes mellitus, insulin-dependent, 2 (IDDM2) [MIM:125852]: A multifactorial disorder of glucose homeostasis that is characterized by susceptibility to ketoacidosis in the absence of insulin therapy. Clinical fetaures are polydipsia, polyphagia and polyuria which result from hyperglycemia-induced osmotic diuresis and secondary thirst. These derangements result in long-term complications that affect the eyes, kidneys, nerves, and blood vessels. Note=The disease is caused by mutations affecting the gene represented in this entry.
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176]: A rare form of diabetes distinct from childhood-onset autoimmune diabetes mellitus type 1. It is characterized by insulin-requiring hyperglycemia that is diagnosed within the first months of life. Permanent neonatal diabetes requires lifelong therapy. Note=The disease is caused by mutations affecting the gene represented in this entry.
Maturity-onset diabetes of the young 10 (MODY10) [MIM:613370]: A form of diabetes that is characterized by an autosomal dominant mode of inheritance, onset in childhood or early adulthood (usually before 25 years of age), a primary defect in insulin secretion and frequent insulin-independence at the beginning of the disease. Note=The disease is caused by mutations affecting the gene represented in this entry.

Similarity:
Belongs to the insulin family.

Database links:

Entrez Gene: 3630 Human

Entrez Gene: 280829 Cow

Entrez Gene: 16333 Mouse

Entrez Gene: 16334 Mouse

Entrez Gene: 24505 Rat

Entrez Gene: 397415 Pig

Omim: 176730 Human

SwissProt: P01308 Human

SwissProt: P01325 Mouse

SwissProt: P01322 Rat

SwissProt: P01315 Pig

Unigene: 272259 Human




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

胰島素(Isulin)胰島素抗體是胰島細胞分泌得一種激素,可以減底血糖濃度。此抗體和人胰島素反應,并與大多數哺乳類動物的胰島素有交叉反應,主要用于胰島細胞瘤的功能性研究。
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: 国产精品亚洲AV三区黑牛牛影视| av资源免费观看试看资源| 国内精品久久久久久99懂色 | 精品人妻无码在线视频导航| 懂色AV色香蕉一区二区蜜桃| 岛国无码在线视频播放网页 | 亚洲精品无码自拍九色窝| 久久熟女嫩草成人片免费| fc2ppv在线观看播放素人| 亚洲∧v久久久无码精品+色欲| 久久成人无码国产免费播放软件| 久久不见久久见免费视频www中字| 非洲AV无码内射| 亚洲国产一成人久久精品,国产成人一区二区三区影院 | 国产香蕉在线精彩视频观看| 一级做a爰全过程免费视频,日韩一区二区三区四区区区 | 久久国产劲暴∨内射 加藤| 2022中文字幕在线观看视频a三区 2022中文字幕在线精品一区二 | 96精品无码成人有声书| 手机在线看片你懂得欧美日韩| 国产成人久久精品二区三区久久_av无码久 | 国产在视频线精品视频,国内精品自线在拍2020| chinese性盛旺55熟女| 日韩一区二区三区免费播放国| 白人狂躁女人高潮视频在线观看| 少妇人妻无码精品视频手机| 成人综合伊人五月婷久久| 日韩精品无码免费专区午夜视频vvv| 丁香五月网久久综合网,狠色伊人亚洲 | 伊人中出激情视频| 精品国产综合区久久久久久_久久精品 | 亚洲卡一卡二在线观看在线视频 | 中文字幕一区二区三匹在线观看| 中文字幕乱码久久午夜69| 久久婷婷五月综合色高清亚洲 | 亚洲精品无码成人AAA片金瓶双娇| 日本视频免费观看MV| 久久午夜精品视频网| 制服.丝袜.亚洲.中文.综合p| 久久久久久亚洲精品成人小说| 中文 无码 在线 97|