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(guān)注公眾號           掃碼咨詢技術(shù)支持           掃碼咨詢技術(shù)服務(wù)
  
客服熱線:400-901-9800  客服QQ:4009019800  技術(shù)答疑  技術(shù)支持  質(zhì)量反饋  人才招聘  關(guān)于我們  聯(lián)系我們
亚洲女人影院想要爱,久久人妻av一区二区软件,男人j进女人p免费视频
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Mouse Anti-Insulin Glargine/BF647 Conjugated antibody (bsm-33122M-BF647)
訂購熱線:400-901-9800
訂購郵箱:sales@www.chomd.com.cn
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@www.chomd.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bsm-33122M-BF647
英文名稱1 Mouse Anti-Insulin Glargine/BF647 Conjugated antibody
中文名稱 BF647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(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領(lǐng)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(yīng)
產(chǎn)品應(yīng)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 Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4.
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:
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(quán)所有 2004-2026 www.www.chomd.com.cn 北京博奧森生物技術(shù)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
主站蜘蛛池模板: 久久综合狠狠综合久久AI换脸| 国产精品JIZZ在线观看软件| 2024国片精品无套内谢无码| 一本色道无码道DVD在线播放直播 一本无码久久久国产Av | 久久亚洲春色中文字幕久久久...| 国精品无码一区二区三区左线 亚洲AV无码专区 | 久久综合亚洲色一区二区三区高清4k| 国语自产精品视频一区二区三区 | 一区二区三区四区在线播放刘嘉玲 | 国产3d同人无遮挡在线观看网站| 亚洲综合国产成人丁香五月激情岁月| 人妖自慰狂喷不止| 成年男人深夜在线视频播放| 亚洲国产成人久久一区二区三区果冻传媒 | 精品无码人妻一区二区三区品_国产免费 | 另类TS人妖一区二区三区| 成年女人AA级毛片免费观看| 亚洲第一页中文字幕在线视频看看| 精品无码国产自产拍在涩| 中国字幕Au7666| 精品乱码一区内射人妻无码高清全集哪里可以看| 北条麻妃国产九九九精品小说 | 99久久亚洲精品无码毛片,国产A级毛片久| 亚洲白虎一区二区白虎一线天 | 亚洲熟女乱综合一区二区!| 狠狠色丁香久久婷婷综_| 亚洲人成电影网站色mp8| 国产日韩精品一区二区三区在线_ 国产日韩精品一区二区三区在线观看婷欧美日韩 | 久久久久久久久久久久久久久精品 | 两个体校校草被C出水尿男男| 俺来也国产区| 裸体孕妇乄乂乄ⅹ乄心| 一本色道视频第一页| 国产午夜精品无码专区在线九九| 亚洲大尺度无码专区尤物,国产情节片| 国产女人aaa级久久久级l久久精品人妻无码一区二区 | 一二三无码视频观看| 国产三级久久精品99舀95pao | 久久精品国产亚洲麻豆小说-91精品一区二区 | 中文字幕岛国高清四季偷拍| 精品一区二区三区在线成人3d动漫|