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视网膜色素变性蛋白4抗体

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产品名称: 视网膜色素变性蛋白4抗体
产品型号: Rhodopsin/RP4/RHO
产品展商: 单克隆抗体/多克隆抗体
产品文档: 无相关文档

简单介绍

视网膜色素变性蛋白4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。视网膜色素变性蛋白4抗体生产每个流程都执行严格的检测标准,保证蛋白抗原产品质量,质量稳定,实验效果明显。


视网膜色素变性蛋白4抗体  的详细介绍

视网膜色素变性蛋白4抗体

规格:1mg/1ml

英文名: Rhodopsin/RP4/RHO

别名: CSNBAD1; MGC138309; MGC138311; OPN 2; OPN2; opsd; OPSD_HUMAN; Opsin 2; opsin 2; Opsin 2 rod pigment; Opsin-2; Opsin2; Retinitis Pigmentosa 4; Retinitis pigmentosa 4 autosomal dominant; RHO; Rhodopsin;

分子量: 39kDa

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

克隆类型:Polyclonal

亚型:IgG

纯化方法:affinity purified by Protein A

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

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

细胞定位:细胞膜

视网膜色素变性蛋白4抗体产品介绍:background: Retinitis pigmentosa is an inherited progressive disease which is a major cause of blindness in western communities. It can be inherited as an autosomal dominant, autosomal recessive, or X-linked recessive disorder. In the autosomal dominant form,which comprises about 25% of total cases, approximately 30% of families have mutations in the gene encoding the rod photoreceptor-specific protein rhodopsin. This is the transmembrane protein which, when photoexcited, initiates the visual transduction cascade. Defects in this gene are also one of the causes of congenital stationary night blindness. [provided by RefSeq, Jul 2008] Function: Photoreceptor required for image-forming vision at low light intensity. Required for photoreceptor cell viability after birth. Light-induced isomerization of 11-cis to all-trans retinal triggers a conformational change leading to G-protein activation and release of all-trans retinal. Subcellular Location: Membrane. Synthesized in the inner segment (IS) of rod photoreceptor cells before vectorial transport to the rod outer segment (OS) photosensory cilia. Tissue Specificity: Rod视网膜色素变性蛋白4抗体 shaped photoreceptor cells which mediates vision in dim light. Post-translational modifications: Phosphorylated on some or all of the serine and threonine residues present in the C-terminal region. DISEASE: Retinitis pigmentosa 4. Night blindness, congenital stationary, autosomal dominant 1. Similarity: Belongs to the G-protein coupled receptor 1 family. Opsin subfamily. Contains one covalently linked retinal chromophore. Gene ID: 6010 Database links: Entrez Gene: 509933 Cow Entrez Gene: 493763 Dog Entrez Gene: 6010 Human Entrez Gene: 212541 Mouse Entrez 视网膜色素变性蛋白4抗体Gene: 24717 Rat Omim: 180380 Human SwissProt: Q95KU1 Cat SwissProt: P28681 Chinese Hamster SwissProt: P02699 Cow SwissProt: P32308 Dog SwissProt: P08100 Human SwissProt: P15409 Mouse SwissProt: P49912 Rabbit SwissProt: P51489 Rat Unigene: 247565 Human Unigene: 2965 Mouse Unigene: 406156 Mouse Unigene: 92530 Rat Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

视网膜色素变性蛋白4抗体品应用: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  神经生物学  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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