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
又爽又黄又无遮挡网站,男人j桶女人p免费视频,国产极品美女高潮抽搐免费网站
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-C1GALT1C1/Gold Conjugated antibody (bs-13801R-Gold)
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(10nm  15nm  35nm
100ul/2980.00元
大包裝/詢價
產品編號 bs-13801R-Gold
英文名稱1 Rabbit Anti-C1GALT1C1/Gold Conjugated antibody
中文名稱 膠體金標記的半乳糖基轉移酶2抗體
別    名 HSPC067; 3-galactosyltransferase 2; Beta 1,3 galactosyltransferase 2; Beta1,3 galactosyltransferase 2; C1Gal T2; C1Gal-T2; C1GALT1 specific chaperone 1; C1GALT1-specific chaperone 1; C1galt1c1; C1GalT2; C1GLC_HUMAN; C38H2 L1; C38H2 like protein 1; C38H2-L1; C38H2-like protein 1; C38H2L1; Core 1 beta1; Core 1 beta3 galactosyltransferase specific molecular chaperone; Core 1 beta3-Gal-T2; Core 1 beta3-galactosyltransferase-specific molecular chaperone; Core 1 UDP galactose:N acetylgalactosamine alpha R beta 1,3 galactosyltransferase 2; COSMC; HSPC067; MGC19947; MGC19947; MST143.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul(10nm  15nm  35nm
研究領域 腫瘤  細胞生物  信號轉導  糖蛋白  新陳代謝  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Horse, Sheep, )
產品應用 IEM=1:20-200 ICA=1:20-200 ChIP=1:20-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 36kDa
性    狀 Lyophilized or Liquid
濃    度 0.4mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human C1GALT1C1
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.02M TBS(pH8.2) with 1% BSA, 0.03% Proclin300.
保存條件 Store at 2-8 oC for 3-6 months. Avoid repeated freeze/thaw cycles.
產品介紹 background:
This gene encodes a type II transmembrane protein that is similar to the core 1 beta1,3-galactosyltransferase 1, which catalyzes the synthesis of the core-1 structure, also known as Thomsen-Friedenreich antigen, on O-linked glycans. This gene product lacks the galactosyltransferase activity itself, but instead acts as a molecular chaperone required for the folding, stability and full activity of the core 1 beta1,3-galactosyltransferase 1. Mutations in this gene have been associated with Tn syndrome. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Dec 2009]

Function:
Probable chaperone required for the generation of 1 O-glycan Gal-beta1-3GalNAc-alpha1-Ser/Thr (T antigen), which is a precursor for many extended O-glycans in glycoproteins. Probably acts as a specific molecular chaperone assisting the folding/stability of core 1 beta-3-galactosyltransferase (C1GALT1).

Subunit:
Associates with core 1 beta-3-galactosyltransferase (C1GALT1), probably not with the soluble active form.

Subcellular Location:
Membrane; Single-pass type II membrane protein (Potential).

Tissue Specificity:
Ubiquitously expressed. Abundantly expressed in salivary gland, stomach, small intestine, kidney, and testis and at intermediate levels in whole brain, cerebellum, spinal cord, thymus, spleen, trachea, lung, pancreas, ovary, and uterus.

DISEASE:
Defects in C1GALT1C1 are the cause of Tn syndrome (TNSYN) [MIM:300622]. Tn syndrome is a rare autoimmune disease caused by somatic mutation in the C1GALT1C1 gene in which subpopulations of blood cells of all lineages carry an incompletely glycosylated membrane glycoprotein, i.e. the Tn antigen. Since leukocytes and platelets are affected as well as red cells, anemia, leukopenia and thrombocytopenia are features. Tn-polyagglutinability is sometimes associated with leukemia or is a preleukemic state.

Similarity:
Belongs to the glycosyltransferase 31 family. Beta3-Gal-T subfamily.

Database links:

Entrez Gene: 29071 Human

Omim: 300611 Human

SwissProt: Q96EU7 Human

Unigene: 643920 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: 一区 二区 三区 中文字幕视频| 18一20女人毛片毛片| 亚洲黄色在线播放动漫| 无码精品人妻一区二区三区漫画 192.168.0.1| 日韩无免费密码视频16| 国产一区二区精品久久岳,精品精品国产自在 | 亚洲无人区一区二区三区app| 色 五月 亚洲 伦伦| 国产97在线观看观看| 亚洲精品秘?无码一区二区软件 | 99精品国产自在现线免费,2021| 亚洲精品一区二区三区在线| 久久99久久99精品免观看软件色情少妞| 婷婷色中文字幕综合在线,电影丰满www | 国产免费无码一区二区军旅片| 在线天堂中文在线资源网8在线中文| 四虎影视永久在线精品2023分集剧情介绍| 国产自啪精品视频网站丝袜app| 亚洲综合自拍成人免费视频网| 久久av午夜色情亚洲剧场| 中文字幕亚洲乱码熟女一区二区图片 | 亚洲中文婷婷888| 狠狠色丁香婷婷久久综合不卡_欧美日韩| 2019天堂精品视频在线观看免费 | 国产婷婷色一区二区三区在线黑人| 一区二区三区视频观看网页| 久久久久久亚洲精品影院 - va天堂久久久久久久久 | 久久久久久久久96浪 | 极品粉嫩小仙女高潮喷水久久动态图 | 精品爆乳一区二区三区无码A∨| 一区二区三区视频观看传媒| 精品国产亚洲一区二区三区久久久久久久久 | heyzo在线播放中文av| 欧美日韩性猛交XXXXX无码视频| 91老熟女玩小伙网| 久久久午夜精品理论片_| 亚洲一区欧洲一区常理6分钟| 国产内射网站免费视频观看 | 亚洲成在人线Av中文字幕h| 成人无码免费一区二区三区免费无码| 人妻少妇精品中文字幕99综合蜜桃|