来一水AV@lysav|亚洲AV无码片VR一区二区三区 |国产亚洲精久久久久久无码|视色4se成人午夜精品久久

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
后入视频在线播放天天干|人物动物交互狗AA|中国人妻被两个老外三P
Mouse Anti-Insulin (1G11)/BF647 Conjugated antibody (bsm-0855M-BF647)
訂購熱線:400-901-9800
訂購郵箱:sales@73327.net
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@73327.net
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號 bsm-0855M-BF647
英文名稱1 Mouse Anti-Insulin (1G11)/BF647 Conjugated antibody
中文名稱 BF647標(biāo)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(guī)格價(jià)格 100ul/2980元 購買        大包裝/詢價(jià)
說 明 書 100ul  
研究領(lǐng)域 腫瘤  心血管  細(xì)胞生物  神經(jīng)生物學(xué)  信號轉(zhuǎn)導(dǎo)  生長因子和激素  糖尿病  內(nèi)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(yīng) (predicted: Human, )
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 5.8/12kDa
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(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.

胰島素(Isulin)胰島素抗體是胰島細(xì)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(yīng),并與大多數(shù)哺乳類動物的胰島素有交叉反應(yīng),主要用于胰島細(xì)胞瘤的功能性研究。
版權(quán)所有 2004-2026 www.73327.net 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
中文字幕一区二区人妻久久精品| 99精品亚洲AV无码国产另类| 久久久无码精品亚洲日韩啪啪网站 | 欧美ZC0O人与善交另类A片| 中日韩V无码中文字幕| 美女视频黄网站免费观看| 国产AV麻豆MAG剧集| 日韩精品人妻一区二区三区蜜桃臀 | 一本大道伊人AV久久综合| 欧美日韩成人在线| 欧美成人一级片在线观看| 偷窥50个美女撒尿高清| 黄色电影免费看| 国产亚洲日韩欧美另类| 人妻少妇久久久久久97人妻| 国模小黎自慰GOGO人体| 韩国三级日本三级人与波| 亚洲18色成人网站WWW| 精品国产96亚洲一区二区三区| 18禁免费高清啪啪网站| 亚洲精久久久久久久| 少妇高潮一区二区三区99| 日日碰狠狠添天天爽无码| 公交车上内裤滑进去了会怎么样 | 亚洲精品久久无码AV片俺去也| 亚洲精品国产精品国自产观看| 男女无遮挡XX00动态图120秒| 亚洲第一AV网站| 国产精品高潮呻吟AV久久动漫| 色99亚洲欧美日韩| 亚洲AV无码一区二区三区乱子伦| 娇妻色情按摩H| 日本一区二区三区视频免费看| 国产婷婷色一区二区三区在线| 精品国产一区二区三区精品| 娇妻借朋友高H繁交H| 精品久久久久久久一区二区2| 国产免费无码一区二区视频| 午夜成熟看A级毛片| 天堂8在线天堂资源BT| 无码精品一区二区三区|