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岩藻糖变旋酶/Fucose mutarotase抗体

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产物名称: 岩藻糖变旋酶/Fucose mutarotase抗体
产物型号: Fukutin
产物展商: 单克隆抗体/多克隆抗体
产物文档: 无相关文档

简单介绍

岩藻糖变旋酶/Fucose mutarotase抗体应用于IHC、WB、 IF、IP、ELISA等科研实验,按理化性质和生物学功能IgM、IgG、IgA、IgE、IgD五类。按抗体的来源,可将其分为天然抗体和**抗体。岩藻糖变旋酶/Fucose mutarotase抗体生产每个流程都执行严格的检测标准,保证蛋白抗原产物质量,质量稳定,实验效果明显。


岩藻糖变旋酶/Fucose mutarotase抗体  的详细介绍

岩藻糖变旋酶/Fucose mutarotase抗体

规格:1尘驳/1尘濒

英文名: Fukutin

别名: C10orf125; Chromosome 10 open reading frame 125; FUCM_HUMAN; Fucose mutarotase; FUCU; Protein fucU homolog.

分子量: 17kDa

储存液:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glyce

克隆类型:笔辞濒测肠濒辞苍补濒

亚型:滨驳骋

纯化方法:affinity purified by Protein A

**原:KLH conjugated synthetic peptide derived from human Fukutin

交叉反应:Human, Mouse, Rat, Dog, Pig, Cow,

细胞定位:

岩藻糖变旋酶/Fucose mutarotase抗体产物介绍:background: Fukutin, a secreted protein, is expressed in various tissues in normal individuals. Fukutin colocalizes with a Golgi marker and a granular cytoplasmic distribution, suggesting that fukutin passes through the Golgi before being packaged into secretory vesicles. Fukutin may be located in the extracellular matrix, where it interacts with and reinforces a large complex encompassing the outside and inside of muscle membranes; alternatively, as a secreted protein, fukutin may cause muscular dystrophy by an unknown mechanism. The fukutin gene is expressed at similar levels in control fetal and brain, but is much reduced in Fukuyama congenital muscular dystrophy (FCMD) brains. Fukutin deficiency affects the modification of glycosylation of DAG1 (α-dystroglycan), which then cannot localize or function properly and may be degraded or eluted from the extracellular surface membrane of the muscle fiber. FCMD is the first human disease known 岩藻糖变旋酶/Fucose mutarotase抗体to be caused by an ancient retrotransposal integration. The gene which encodes fukutin maps to human chromosome 9q31. Function: Involved in the interconversion between alpha- and beta-L-fucoses. L-Fucose (6-deoxy-L-galactose) exists as alpha-L-fucose (29.5%) and beta-L-fucose (70.5%), the beta-form is metabolized through the salvage pathway. GDP-L-fucose formed either by the de novo or salvage pathways is transported into the endoplasmic reticulum, where it serves as a substrate for N- and O-glycosylations by fucosyltransferases岩藻糖变旋酶/Fucose mutarotase抗体. Fucosylated structures expressed on cell surfaces or secreted in biological fluids are believed to play a critical role in cell-cell adhesion and recognition processes. Subunit: Mainly homodimer, but exists also as homotetramer, homooctamer, and homodecamer. The homodimeric form seems catalytically inactive (By similarity). Similarity: Belongs to the rbsD / fucU family. Database links: Entrez Gene: 282969 Human SwissProt: A2VDF0 Human Unigene: 155823 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

岩藻糖变旋酶/Fucose mutarotase抗体产物应用:WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (石蜡切片需做抗原修复) not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.

研究领域:细胞生物  信号转导  

储存条件: Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

来源: Rabbit

外观: Lyophilized or Liquid


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