加入收藏
百奥莱博公司客服电话百奥莱博QQ百奥莱博QQ百奥莱博QQ
百奥莱博公司微信服务号

产品目录

所在位置:所有产品 > 抗体抗原 > 一抗 > GALE抗体
GALE抗体图片
产品货号:
Z37667
中文名称:
GALE抗体
英文名称:
Anti-GALE Antibody (Clone#OTI1C4)
产品规格:
50μl|100μl|150μl
发货周期:
1~3天
产品价格:
询价
抗体名称Anti-GALE Antibody (Clone#OTI1C4)
指标别名Galactowaldenase;GALE;SDR1E1;UDP glucose 4 epimerase;UDP-galactose-4-epimerase
克隆性Monoclonal
检验物种human,monkey,mouse,rat,dog
应用范围WB,IHC
基因名称GALE
克隆号OTI1C4
抗体来源Mouse
抗体类型IgG1
免疫原Full length human recombinant protein of human GALE (NP_000394) produced in HEK293T cell.
实际分子量38.1KD
成分PBS (PH 7.3) containing 1% BSA,50% glycerol and 0.02% sodium azide.
纯化方式Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)
浓度500μg/mL
产品形态溶液
保存条件Stable for 12 months from date of receipt.Store at -20℃ as received.
背景资料This gene encodes UDP-galactose-4-epimerase which catalyzes two distinct but analogous reactions:the epimerization of UDP-glucose to UDP-galactose,and the epimerization of UDP-N-acetylglucosamine to UDP-N-acetylgalactosamine.The bifunctional nature of the enzyme has the important metabolic consequence that mutant cells (or individuals) are dependent not only on exogenous galactose,but also on exogenous N-acetylgalactosamine as a necessary precursor for the synthesis of glycoproteins and glycolipids.Mutations in this gene result in epimerase-deficiency galactosemia,also referred to as galactosemia type 3,a disease characterized by liver damage,early-onset cataracts,deafness and mental retardation,with symptoms ranging from mild ('peripheral' form) to severe ('generalized' form).Multiple alternatively spliced transcripts encoding the same protein have been identified.[provided by RefSeq,Jul 2008]
Uniprot IDQ14376
基因名全称UDP-galactose-4-epimerase
蛋白名全称UDP-glucose 4-epimerase
推荐稀释比
Western blot (WB) 1:500~2000
Immunohistochemistry in paraffin section (IHC) 1:150

相关搜索:GALE抗体GALE单抗Anti-GALE Antibody (Clone#OTI1C4)
首页 |  关于我们 |  联系我们 |  在线咨询 |  网站地图
北京百奥莱博科技有限公司 京ICP备14007103号-3