97久久久精品综合88久久_亚洲国产精品一_久热热国产久热_97操操操_北条麻妃在线免费观看_精品国自产拍天天拍

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
欧美做受高潮1,国产香蕉视频上线免费,四虎影院2019
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-GLUT1/PE-Cy7 Conjugated antibody (bs-4855R-PE-Cy7)
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-4855R-PE-Cy7
英文名稱 Rabbit Anti-GLUT1/PE-Cy7 Conjugated antibody
中文名稱 PE-Cy7標記的葡萄糖轉運蛋白1抗體
別    名 Glucose Transporter GLUT1; GT-1; GLUT-1; GLUT 1; Solute carrier family 2; facilitated glucose transporter member 1; Glucose transporter type 1; erythrocyte/brain; DYT17; DYT18; Erythrocyte/brain HepG2 glucose transporter; Erythrocyte/hepatoma glucose transporter; Glucose transporter 1; Glucose transporter type 1; Glucose transporter type 1 erythrocyte/brain; Glucose transporter type 1, erythrocyte/brain; GLUT; GLUT1; GLUT1DS; GLUTB; GT1; GTG1; Gtg3; GTR1_HUMAN; HepG2 glucose transporter; MGC141895; MGC141896; PED; RATGTG1; SLC2A 1; SLC2A1; Solute carrier family 2 (facilitated glucose transporter), member 1; Solute carrier family 2 facilitated glucose transporter member 1.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 腫瘤  細胞生物  免疫學  生長因子和激素  轉運蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Rabbit, Sheep, Guinea Pig, )
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 54kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human GLUT1 (251-320aa)
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:
This gene encodes a major glucose transporter in the mammalian blood-brain barrier. Mutations in this gene have been found in a family with paroxysmal exertion-induced dyskinesia. [provided by RefSeq, Jul 2008].

Function:
Facilitative glucose transporter. This isoform may be responsible for constitutive or basal glucose uptake. Has a very broad substrate specificity; can transport a wide range of aldoses including both pentoses and hexoses. Subcellular location is at Cell membrane; multi-pass membrane protein. Facilitative glucose transporter. This isoform may be responsible for constitutive or basal glucose uptake. Has a very broad substrate specificity; can transport a wide range of aldoses including both pentoses and hexoses.

Subcellular Location:
Cell membrane; Multi-pass membrane protein. Melanosome. Note=Localizes primarily at the cell surface. Identified by mass spectrometry in melanosome fractions from stage I to stage IV.

Tissue Specificity:
Expressed at variable levels in many human tissues.

Post-translational modifications:
Phosphorylated upon DNA damage, probably by ATM or ATR.

DISEASE:
Defects in SLC2A1 are the cause of GLUT1 deficiency syndrome type 1 (GLUT1DS1) [MIM:606777]; also known as blood-brain barrier glucose transport defect. A neurologic disorder showing wide phenotypic variability. The most severe 'classic' phenotype comprises infantile-onset epileptic encephalopathy associated with delayed development, acquired microcephaly, motor incoordination, and spasticity. Onset of seizures, usually characterized by apneic episodes, staring spells, and episodic eye movements, occurs within the first 4 months of life. Other paroxysmal findings include intermittent ataxia, confusion, lethargy, sleep disturbance, and headache. Varying degrees of cognitive impairment can occur, ranging from learning disabilities to severe mental retardation.
Defects in SLC2A1 are the cause of GLUT1 deficiency syndrome type 2 (GLUT1DS2) [MIM:612126]. A clinically variable disorder characterized primarily by onset in childhood of paroxysmal exercise-induced dyskinesia. The dyskinesia involves transient abnormal involuntary movements, such as dystonia and choreoathetosis, induced by exercise or exertion, and affecting the exercised limbs. Some patients may also have epilepsy, most commonly childhood absence epilepsy. Mild mental retardation may also occur. In some patients involuntary exertion-induced dystonic, choreoathetotic, and ballistic movements may be associated with macrocytic hemolytic anemia.

Similarity:
Belongs to the major facilitator superfamily. Sugar transporter (TC 2.A.1.1) family. Glucose transporter subfamily.

Database links:

Entrez Gene: 6513 Human

Entrez Gene: 20525 Mouse

Entrez Gene: 24778 Rat

Omim: 138140 Human

SwissProt: P11166 Human

SwissProt: P17809 Mouse

SwissProt: P11167 Rat

Unigene: 473721 Human

Unigene: 721551 Human

Unigene: 21002 Mouse

Unigene: 3205 Rat

 



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

GLUT-1屬于溶質運載蛋白家族成員(solute carrier family),主要功能是轉載葡萄糖進入上皮細胞。
目前主要用于糖尿病腎病和視網膜病變的研究,也是腎小球系膜細胞上的主要葡萄糖轉運體。GLUT1的功能狀態直接影響系膜細胞的糖代謝及功能變化。
近期,研究人員也用來區別一些良、惡性腫瘤的鑒別。
版權所有 2004-2026 www.kastlife.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: 久久久无码精品亚洲欧美 | www.天天射.com | 成年日韩片AV在线网站医生 | 亚洲三级中文字幕在线看 | 免费不卡欧美自拍视频 | 大地资源在线观看免费高清动漫 | 成人午夜免费无码视频在线观看 | 中文字幕在线观看第三页 | 麻豆少妇厨房com | 亚洲女v | 久久WWW成人看片免费不卡 | 国产无遮挡又黄又爽奶头 | www.夜夜| 玩麻豆国产?片对白日逼视频 | 日韩欧美大片在线观看 | 国产福利男女XX00视频 | 欧美一性一交一A片费看 | 国产精品毛片一区二区 | 91精选在线观看 | 又大又粗又爽免费视频a片 婷婷五月综合丁香在线 | 精品久久久久久久久久中文字幕 | 毛片在线看片 | 在线中文av| 欧美精品高清 | 在线观看国产成人av天堂 | 久久久久国色AⅤ免费看 | 欧美性生交大片免费看a片 黄色录像a级片 | 97色成人网 | 女人自慰片免费观看 | 91久久国产综合久久91精品网站 | 夜夜澡人摸人人添人人看 | 色八a级在线观看 | 午夜视频福利网站 | 亚洲欧美日韩在线 | 成年人国产网站 | 韩国日本三级在线 | 日日噜狠狠噜天天噜AV | 国产九色在线 | av网页观看 | 成人一级视频 | 免费网站www在线观看 |