强伦轩一级A片在线观看,中文字幕乱码人妻二区三区,鲁鲁狠狠狠7777一区二区,西西4444www无码精品
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  關于我們  聯系我們
农村妇女亂伦91熟妇,成人免费黄色视频
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-CHST6/Cy5.5 Conjugated antibody (bs-13937R-Cy5.5)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-13937R-Cy5.5
英文名稱 Rabbit Anti-CHST6/Cy5.5 Conjugated antibody
中文名稱 Cy5.5標記的碳水化合物磺基轉移酶6抗體
別    名 C GlcNAc6ST; C-GlcNAc6ST; Carbohydate sulfotransferase 6; Carbohydrate (N acetylglucosamine 6 O) sulfotransferase 6; Carbohydrate sulfotransferase 6; CHST6; CHST6_HUMAN; Corneal GlcNAc6-sulfotransferase; Corneal N acetylglucosamine 6 sulfotransferase; Corneal N-acetylglucosamine-6-O-sulfotransferase; Galactose N acetylglucosamine N acetylglucosamine 6 O sulfotransferase 4 beta; Galactose/N-acetylglucosamine/N-acetylglucosamine 6-O-sulfotransferase 4-beta; GlcNAc6ST 5; GlcNAc6ST-5; Gn6st-5; GST4 beta; GST4-beta; hCGn6ST; N-acetylglucosamine 6-O-sulfotransferase 5.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 神經生物學  細胞類型標志物  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human,  (predicted: Dog, Cow, Horse, Sheep, )
產品應用 ICC=1:50-200 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 44kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human CHST6
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.
產品介紹 background:
The protein encoded by this gene is an enzyme that catalyzes the transfer of a sulfate group to the GlcNAc residues of keratan. Keratan sulfate helps maintain corneal transparency. Defects in this gene are a cause of macular corneal dystrophy (MCD). [provided by RefSeq, Jan 2010]

Function:
Sulfotransferase that utilizes 3'-phospho-5'-adenylyl sulfate (PAPS) as sulfonate donor to catalyze the transfer of sulfate to position 6 of non-reducing N-acetylglucosamine (GlcNAc) residues of keratan. Mediates sulfation of keratan in cornea. Keratan sulfate plays a central role in maintaining corneal transparency. Acts on the non-reducing terminal GlcNAc of short and long carbohydrate substrates that have poly-N-acetyllactosamine structures.

Subcellular Location:
Golgi apparatus membrane.

Tissue Specificity:
Expressed in cornea. Mainly expressed in brain. Also expressed in spinal cord and trachea.

DISEASE:
Defects in CHST6 are the cause of macular dystrophy, corneal, 1 (MCDC1) [MIM:217800]. An ocular disease characterized by bilateral, progressive corneal opacification, and reduced corneal sensitivity. Onset occurs in the first decade, usually between ages 5 and 9. Painful attacks with photophobia, foreign body sensations, and recurrent erosions occur in most patients. The disease is due to deposition of an unsulfated keratan sulfate both within the intracellular space (within the keratocytes and endothelial cells) and in the extracellular corneal stroma. Macular corneal dystrophy is divided into the clinically indistinguishable types I, IA, and II based on analysis of the normally sulfated, or antigenic, keratan sulfate levels in serum and immunohistochemical evaluation of the cornea. Patients with types I and IA macular corneal dystrophy have undetectable serum levels of antigenic keratan sulfate, whereas those with type II macular corneal dystrophy have normal or low levels, depending on the population examined. Note=CHST6 homozygous missense mutations have been observed in patients with macular corneal dystrophy type I, while type II patients show a large deletion and replacement in the upstream region of CHST6. The only missense mutation for type II is Cys-50, which is heterozygous with a replacement in the upstream region on the other allele of CHST6.

Similarity:
Belongs to the sulfotransferase 1 family. Gal/GlcNAc/GalNAc subfamily.

Database links:

Entrez Gene: 4166 Human

Omim: 605294 Human

SwissProt: Q9GZX3 Human

Unigene: 655622 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.nmgps.com 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(yī)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
91少妇高潮呻吟无码精品 | 亚洲精品久久久久久久久久飞鱼 | 免费在线观看AV | 麻豆乱码国产一区二区三区 | 国产精品伦子伦免费视频 | 欧美激情一区二区不卡 | 欧美激情无码视频一二三 | 东北女人逼毛多水多大片 | 三级片网站在线观看 | 国产传媒免费观看AV | 国产高清在线观看 | 看得你下面流水视频 | 亂倫國產一級生活片免費 | 免费 无码 国产免费 | 好爽好大久久久级婬片毛片 | 91麻豆精品久久久久蜜臀 | 西西4444WWW无码精品 | 亚洲国产婷婷香蕉久久久久久99 | 久久精品人妻一区二区三区宅男必备 | 免费h视频在线观看 | 人妻纶乱A级毛片免费看初女 | 久久水蜜臀亚洲AV无码精品 | 一本一道久久综合狠狠躁牛牛影视 | 日本精品久久久久中文人妻 | 品善网AV无码在线播放 | 又硬又粗的a级少妇毛片 | 波多野结衣 一区 二区 | 伦伦影院午夜理论片痴汉 | 无码精品一区二区三区四区爱奇艺 | 丰满人妻被猛烈进入中文字幕 | 鲁大师免费观看日本电影 | 免费亲子乱婬一级A片 | 又黄又粗又猛国产免费 | 超碰在线免费成人WWW | 日韩人妻免费内射 | 一级毛片久久久久久久女人18 | 91丨国产丨白浆秘 洗澡吊死 | 国产又黄又硬又粗又爽高清红挑 | 久久国产精品一区二区 | 久久人妻嫩草无码AV专区动漫 | 国产女性无套免费网站 |