Gene ID: 5160 种属 Homo sapiens 基因序列编号: NM_000284.4 基因描述 Homo sapiens pyruvate dehydrogenase E1 subunit alpha 1 (PDHA1), transcript variant 1, mRNA; nuclear gene for mitochondrial product DNA编码区: atgaggaagatgctcgccgccgtctcccgcgtgctgtctggcgcttctcagaagccggca agcagagtgctggtagcatcccgta...
PDHA1[HGNC][GeneCards][NCBI] 基因种类(locus group) protein-coding gene 同源简称(alias symbol) 基因家族代码(gene_family_id) [HGNC][GenScript] omim代码 300502 entrez码 5160[Vega] ensembl基因码 ENSG00000131828[Ensembl] 基因家族(gene family) ...
J. 2010 Sequence variations of PDHA1 gene in Triticeae species allow for iden- tifying wheat-alien introgression lines. Front. Agric. China 4, 137-144.Sequence variations of PDHA1 gene in Triticeae species allow for identifying wheat-alien introgression lines[J] . Juqing Jia,Guangrong Li,...
(-20℃) 相关类别: 抗原 概述: Fusion protein corresponding to a region derived from 191-390 amino acids of human PDHA1 技术规格: Full name: Synonyms: Swissprot: Gene Accession: Purity: Expression system: Tags: Background: pyruvate dehydrogenase E1 alpha 1 subunit PDHA; PDHAD; PHE1A; PDHCE...
Methods Polymerase chain reaction (PCR) was performed to amplify the 11 exons and exon junction of the PDHA1 gene from a child who was diagnosed with PHD based on clinical characteristics and laboratory examination results. The PCR products were sequenced to determine the mutation. An analysis of...
(iΔEC/-) 小鼠 图 1 |新生小鼠基因鉴定结果以及小鼠的体型及体质量 Figure 1 | Gene identification results of newborn mice and their body size and body mass 2.2 小鼠肺组织中的 PDHA1 蛋白表达水平 PDHA1(iΔEC/iΔEC) 条件性 敲除小鼠的PDHA1蛋白相对表达量低于PDHA1(iΔEC/-) 小鼠(t=4.320,...
提供的PDHA1单克隆抗体产品克隆号为,对应的亚型为。该基因又称PDHA|PDHCE1A|PHE1A,全名为pyruvate dehydrogenase (lipoamide) alpha 1,对应Gene号为,其蛋白编号为P08559;NM_000284。3。 应用类型 ELISA,WB-Ce 免疫原 Recombinant protein corresponding to C-terminus of human PDHA1。
Gene Ontology富集分析表明差异修饰蛋白的主要生物学过程涉及细胞呼吸、三羧酸循环(TCA)和氧化磷酸化(图1E)。据报道,在 SAKI 发育过程中,肾小管上皮细胞中脂肪酸氧化和 TCA 受到抑制,而糖酵解增强。因此,在参与这些代谢过程的差异蛋白中,PDHA1作为糖酵解和TCA之间的第一个关键限速酶引起了作者的注意(图1F)。
Gene mutation detection of one patient with pyruvate dehydrogenase complex deficiency by using next generation sequencing 丙酮酸脱氢酶复合体缺乏症.诊断明确后,经维生素B1,辅酶Q10,左旋肉碱等治疗3个月,患儿运动能力显著改善,病情稳定.结论PDHA1基因突变所致的丙酮酸脱氢酶复合体缺乏症... S Liu,J Liang,H Ouy...
货号产品名称Method规格价格货期 CDS-H09617-1pDonR223-PDHA1GateWay2ug/0.5ml￥800现货 CDS-H09617-2pMD18-T-PDHA1TA克隆2ug/0.5ml￥800-15001-2周 PDHA1 重组病毒 货号产品名称Method规格价格货期 CDS-H09617-11rAd-PDHA1重组腺病毒10^10cfu/支￥30003-5周 ...