Gene SummaryThis gene encodes one of the SERCA Ca(2+)-ATPases, which are intracellular pumps located in the sarcoplasmic or endoplasmic reticula of muscle cells. This enzyme catalyzes the hydrolysis of ATP coupled with the translocation of calcium from the cytosol to the sarcoplasmic reticulum lum...
Gene Summary This gene encodes one of the SERCA Ca(2+)-ATPases, which are intracellular pumps located in the sarcoplasmic or endoplasmic reticula of muscle cells. This enzyme catalyzes the hydrolysis of ATP coupled with the translocation of calcium from the cytosol to the sarcoplasmic reticulum ...
Contreras‑Leal E, Hernandez‑Oliveras A, Flores‑Peredo L, Zarain‑Herzberg A and Santiago‑Garcia J: Histone deacetylase inhibitors promote the expression of ATP2A3 gene in breast cancer cell lines. Mol Carcinog 55: 1477‑1485, 2016....
提供的ATP2A3人源重组蛋白(Q01)产品为带有GST标签的人源ATP2A3部分序列重组蛋白,其对应的GeneID号为489。 产品描述 与其它公司提供的重组蛋白不同,该ATP2A3人源重组蛋白(Q01)产品为采用CFS的无细胞麦胚蛋白合成系统表达出来的重组蛋白,可表达出对细胞有毒性、易被蛋白酶降解的蛋白;并获得具有良好的可溶性,并有翻...
This product contains 3 separate slightly different shRNA sequences which knock down rat ATP2A3 gene specifically. Each vial contains 50 μg of lyophilized shRNA. Target Rat ATP2A3 Reactivity Rat Host E. coli Tested Applications RNAi Form Lyophilized Specificity ATP2A3 shRNA Plasmid (Rat) ...
This gene encodes one of the SERCA Ca(2+)-ATPases, which are intracellular pumps located in the sarcoplasmic or endoplasmic reticula of muscle cells. This enzyme catalyzes the hydrolysis of ATP coupled with the translocation of calcium from the cytosol to the sarcoplasmic reticulum lumen, and is...
Gene Info — ATP2A3 Interactomes Pathways Diseases Related Products H00000489-M01 ATP2A3 monoclonal antibody (M01), clone 2H3 H00000489-W01P ATP2A3 DNAxPab H00000489-K ATP2A3 rabbit monoclonal antibody H00000489-B01P ATP2A3 purified MaxPab mouse polyclonal antibody (B01P)...
The protein encoded by this gene belongs to the family of P-type primary ion transport ATPases characterized by the formation of an aspartyl phosphate intermediate during the reaction cycle. These enzymes remove bivalent calcium ions from eukaryotic cells against very large concentration gradients and...
该突变为错义突变,虽然在人类基因突变数据库(Human Gene Mutation Database,HGMD)专业版数据库中尚未见报道,但由于其不属于多态性位点,在人群中发生频率极低,且结合患儿临床有交替性偏瘫的表现,故考虑为致病突变。父母均未检测到此突变,考虑为新发突变。 诊断后予以氟桂利嗪10 mg/d治疗及妥泰抗癫痫治疗,随访1年,...
At this date, 173 loci of deafness gene have been reported in the literature (69 DFNA, 94 DFNB, 6 X-linked DFN, 2 DFNM, 1 DFNY and 1 AUNA1). For syndromic deafness, approximately 400 syndromes associated with hearing disorders are already described. Thus, the determination of causal ...