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
色欲色香天天天综合vvv,日韩激情无码免费毛片,a国产成人免费视频
首頁 > 產品中心 > 標記一抗 > 產品信息
Mouse Anti-Insulin Glargine/Cy3 Conjugated antibody (bsm-33122M-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-33122M-Cy3
英文名稱1 Mouse Anti-Insulin Glargine/Cy3 Conjugated antibody
中文名稱 Cy3標記的甘精胰島素
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 生長因子和激素  糖尿病  
抗體來源 Mouse
克隆類型 Monoclonal
克 隆 號 5F12
交叉反應
產品應用
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 5.8kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 Insulin Glargine
亞    型 IgG
純化方法 affinity purified by Protein G
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.
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: 精品久久久久久成人热,91| 国产精品视频一区九色17c| 在线看片毛片无码永久免费监控摄像| 伊人无码在线观看导航| 三上悠亚日韩在线中文| 国产亚洲欧洲精品区 | 制服.丝袜.亚洲.中文.综合p| 午夜樱花视频在线观看网站| 极品人妻av一区二区三区,亚洲日韩av | 图片区 视频区 小说区 SM专区 | 亚洲国产一成人久久精品,亚洲国产成人 | 老太业余BB大全视频 | 一区二区三区久久精品专区| 欧美一区日本一区韩国一区| 东京热女大交乱| 无码日韩人妻精品久久蜜桃免费AV | 色噜噜狠狠狠综合曰曰曰一二本 | 波多野结衣区视频在线播放| 香蕉在线精品视频在线观看2019 | 自拍偷在线精品自拍偷99,日韩好精品视频你懂的 | 里番人妻过夜1—2集| 18禁止看的免费污网站 快播| 日韩精品无码熟人妻视频—本大道| 成人午夜精品无码区久久中文??| 丝袜精品一区二区视频| 99国产精品午夜视频青椒TV| 老熟妇网站年轻人| 亚洲中文字幕精品久久久久久精品久| 精品人体无码一区二区三区加勒比女海盗| 伊人久久综合热线大杳蕉伊9| 精品久久久久影院优,无码精品人妻一区二区 | 黑人巨大20P| 窝窝人体艺7777777 | 一级毛片在线播放免费播放视频w| 久久精品免费一区二区喷水 | 99re这里只有精品6一区| 久久综合婷婷丁香五月天| 一本色道视频第一页| 国产成人精品一区在线网站| 日日婷婷夜日日天干,香蕉久久一区二区...| 超碰人妻日韩一本到|