产品货号:jlcR4041 英文名称 :Transaldolase 1 中文名称 :转醛醇酶/EPS8L2抗体 别 名 :Dihydroxyacetone transferase; EPS8L2; Glycerone transferase; TAL; TAL H; TALDO; TALDO1; TALDOR; TALH; Transaldolase 1; Transaldolase1; Transaldolase-1; EC 2.2.1.2; TALDO_HUMAN. 研究领域 :肿瘤 细胞生物 免疫学 神经生物学 抗体来源 :Rabbit 克隆类型 :Polyclonal 交叉反应 : Human, Mouse, Rat, Dog, Cow, Horse, Sheep, 产品应用 :WB=1:500-2000 ELISA=1:500-1000 IHC-P=1:400-800 IHC-F=1:400-800 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. 分 子 量 :37kDa 细胞定位 :细胞浆 性 状 :Lyophilized or Liquid 浓 度 :1mg/ml 免 疫 原 :KLH conjugated synthetic peptide derived from human Transaldolase 1:145-250/337 亚 型 :IgG 纯化方法 :affinity purified by Protein A 储 存 液 :0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. 保存条件 :Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C. PubMed :PubMed 产品介绍 : Transaldolase 1 is a key enzyme of the nonoxidative pentose phosphate pathway providing ribose-5-phosphate for nucleic acid synthesis and NADPH for lipid biosynthesis. This pathway can also maintain glutathione at a reduced state and thus protect sulfhydryl groups and cellular integrity from oxygen radicals. The functional gene of transaldolase 1 is located on chromosome 11 and a pseudogene is identified on chromosome 1 but there are conflicting map locations. The second and third exon of this gene were developed by insertion of a retrotransposable element. This gene is thought to be involved in multiple sclerosis.
Function: Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway.
Subunit: Homodimer.
DISEASE: Transaldolase 1 deficiency (TALDO1 deficiency) [MIM:606003]: Results in telangiectases of the skin, hepatosplenomegaly, and enlarged clitoris. Note=The disease is caused by mutations affecting the gene represented in this entry.
SWISS: Q9H6S3
Gene ID: 64787
Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.