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
97色偷偷色噜噜狠狠爱网站97,亚洲午夜久久久影院,國产一二三内射在线看片
首頁 > 產品中心 > 標記一抗 > 產品信息
Mouse Anti-Insulin Glargine/FITC Conjugated antibody (bsm-33122M-FITC)
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-FITC
英文名稱1 Mouse Anti-Insulin Glargine/FITC Conjugated antibody
中文名稱 FITC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: 亚洲精品中文字幕乱码无线|亚 | 中文字幕亚洲综合精品一区99精品久久中文字幕日韩精品 | 中文字幕人成无码人妻欧美日韩二区 | 成人精品视频99在线观看免费 | 中文字幕av无码不卡免费,亚洲成av人片不卡无码3D | 日本熟妇Pion| 国产拍拍拍拍拍拍拍射精黄片| 又大又爽又深又无遮挡免费视频| 三上悠亚 亚洲一区二区三区 在线 | 中文字幕无码不卡一区二区三区手机在线观看 | 久久国产护士视频| 中文字幕乱码人妻无码久久久1.每日更新 | 一区二区三区四区在线播放刘嘉玲| 日韩精品一区二区三区老鸭窝三浦理惠子 | 久久精品一区二区三区AⅤ 鲁丝一区 | 色丁香开心网站婷婷月天亚洲| 国产三级久久精品99舀95pao| 亚洲人成无码网站玖玖99热国产| 久久精品一区二区国产全集免费观看| 91精品国产自产91精品资源,色综合久 | 在线精品亚洲一区二区听书| 久久噜噜噜精品国产亚洲综合| 97久久久久亚洲vA无码区首页 | 国产一二三区在线观看thp| 亚洲午夜在线播放教| 国内精品伊人久久久久网站_第38集| 中文字幕精品一区二区精品5566 | 久久久99精品成人片女同中文字幕| 中文字幕av无码不卡免费,亚洲成av人片不卡无码3D | 狠狠亚洲狠狠欧洲熟女| 亚洲熟妇无码av影音先锋影院| 精品偷自拍另类在线观看网址| 亚洲一区二区三区乱码漫画免费 | 色爽黄1000部免费软件下载入囗| 岛国无码在线观看视频在线播放 | 久久精品中文字幕码麻豆发布| 亚洲伊人青青草无码综合视频| 国产午夜亚洲精品国产成人小说-hd黑人三区漫画free... | 国产无遮挡成人免费视频网站的软件 | 人妻无码中文字幕按摩番号| 在线观看动漫aV游戏|