已关闭
  • 顶部Banner位
  • 固定模块
设置
BPD
试用
AI
企业管理端
厂家
GALE Rabbit pAb, AP conjugated
收藏 收藏
分享
需招商
原料试剂 研发实验室
价格
¥2980.00
品牌 Bioss博奥森生物
地区 中国,北京,北京市
货号 bs-13265R-AP
产地 国产
选择规格
100ul
易享客服
Bioss博奥森生物
北京博奥森生物技术有限公司
北京
营业执照已审核
博奥森:专注科研,以优质抗体引领未来 博奥森生物,自2001年诞生以来,始终坚守在生命科学前沿,为全球科研人员提供卓越品质的免疫学试剂产品与服务。我们拥有资深的科学家团队、先进的抗体发现、验证与生产平台,始终坚持“自主研发、原始创新”的理念,确保每一款产品都能达到国际标准,持续提供“4R” 品质科研工具【Repeatable(可重复)、Replicable(可复制)、Reproducible(可再现)和Reliable(可靠的)】。
进入店铺
产品规格 图文详情 技术文档
产品规格
品牌名称
Bioss博奥森生物
货号
bs-13265R-AP
国产/进口
国产
规格
100ul
储存条件
Shipped at 4℃. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
使用范围
WB
货源
新品
图文详情
Application:WB
Reactivity: Mouse (predicted: Human,Rat,Pig,Horse)
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]
技术文档
没有您想要的资料?去索要
返回顶部