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溶质载体转运蛋白家族29成员3抗体

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产品名称: 溶质载体转运蛋白家族29成员3抗体
产品型号: SLC29A3
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

溶质载体转运蛋白家族29成员3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。溶质载体转运蛋白家族29成员3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。


溶质载体转运蛋白家族29成员3抗体  的详细介绍

溶质载体转运蛋白家族29成员3抗体

规格:1mg/1ml

英文名: SLC29A3

别名: Equilibrative nucleoside transporter 3; hENT3; Solute carrier family 29 member 3; ENT3.

分子量: 52kDa

储存液:Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M

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 SLC29A3

交叉反应:Human, Mouse, Rat,

细胞定位:细胞膜

溶质载体转运蛋白家族29成员3抗体产品介绍:Function: Mediates both influx and efflux of nucleosides across the membrane (equilibrative transporter). Mediates transport of adenine, adenosine and uridine, as well as several nucleoside analog drugs, such as anticancer and antiviral agents, including cladribine, cordycepin, tubercidin and AZT. Does not transport hypoxanthine. Tissue Specificity: Widely expressed in both ***** and fetal tissues. Highest levels in placenta, uterus, ovary, spleen, lymph node and bone marrow. Lowest levels in brain and heart. DISEASE: The disease is caused by mutations affecting the gene represented in this entry. Disease description:A syndrome characterized by the combination of features from 2 or more of four histiocytic disorders, originally thought to be distinct: Faisalabad histiocytosis (FHC), sinus histiocytosis with massive lymphadenopathy (SHML), H syndrome, and pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome (PHID). 溶质载体转运蛋白家族29成员3抗体FHC features include joint deformities, sensorineural hearing loss, and subsequent development of generalized lymphadenopathy and swellings in the eyelids that contain histiocytes. SHML causes lymph node enlargement in children frequently accompanied by fever, leukocytosis, elevated erythrocyte sedimentation rate, and polyclonal hypergammaglobulinemia. H syndrome is characterized by cutaneous溶质载体转运蛋白家族29成员3抗体 hyperpigmentation and hypertrichosis, hepatosplenomegaly, heart anomalies, and hypogonadism; hearing loss is found in about half of patients. PHID is characterized by predominantly antibody-negative insulin-dependent diabetes mellitus associated with pigmented hypertrichosis and variable occurrence of other features of H syndrome. Similarity: Belongs to the SLC29A/ENT transporter (TC 2.A.57) family. Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

溶质载体转运蛋白家族29成员3抗体产品应用: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  信号转导  转运蛋白  

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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