MDH2 Antibody
-
货号:CSB-PA013623ESR2HU
-
规格:¥440
-
促销:
-
图片:
-
其他:
产品详情
-
产品名称:Rabbit anti-Homo sapiens (Human) MDH2 Polyclonal antibody
-
Uniprot No.:P40926
-
基因名:MDH2
-
别名:M MDH antibody; Malate dehydrogenase 2; NAD (mitochondrial) antibody; Malate dehydrogenase antibody; Malate dehydrogenase; mitochondrial antibody; MDH antibody; mdh2 antibody; MDHM_HUMAN antibody; MGC:3559 antibody; mitochondrial antibody; Mitochondrial malate dehydrogenase 2; NAD antibody; Mor 1 antibody; MOR1 antibody
-
宿主:Rabbit
-
反应种属:Human, Mouse
-
免疫原:Recombinant Human Malate dehydrogenase, mitochondrial protein (59-338AA)
-
免疫原种属:Homo sapiens (Human)
-
标记方式:Non-conjugated
-
克隆类型:Polyclonal
-
抗体亚型:IgG
-
纯化方式:Antigen Affinity Purified
-
浓度:It differs from different batches. Please contact us to confirm it.
-
保存缓冲液:PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
-
产品提供形式:Liquid
-
应用范围:ELISA, WB
-
推荐稀释比:
Application Recommended Dilution WB 1:500-1:5000 -
Protocols:
-
储存条件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
-
货期:Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
相关产品
靶点详情
-
基因功能参考文献:
- these data suggest that MDH2, functioning as an RNA-binding protein, is involved in the posttranscriptional downregulation of SCN1A expression under seizure condition. PMID: 28433711
- loss-of-function mutations in MDH2 are also associated with severe neurological clinical presentations in children PMID: 27989324
- Data indicate that acetyl-CoA acetyltransferase (ACAT1) and malate dehydrogenase (MDH2) are involved in various drug-resistance-forming mechanisms. PMID: 25639359
- Segregation of the mutation with disease and absence of MDH2 in mutated tumors revealed MDH2 as a novel pheochromocytoma/paraganglioma susceptibility gene. PMID: 25766404
- L-2-hydroxyglutarate accumulates as a result of a deficiency in FAD-linked L-2-hydroxyglutarate dehydrogenase. mitochondrial L-malate dehydrogenase is responsible for the excretion of L-2-hydroxyglutarate in this condition. PMID: 17603759
显示更多
收起更多
-
相关疾病:Epileptic encephalopathy, early infantile, 51 (EIEE51)
-
亚细胞定位:Mitochondrion matrix.
-
蛋白家族:LDH/MDH superfamily, MDH type 1 family
-
数据库链接:
HGNC: 6971
OMIM: 154100
KEGG: hsa:4191
STRING: 9606.ENSP00000327070
UniGene: Hs.520967
Most popular with customers
-
-
YWHAB Recombinant Monoclonal Antibody
Applications: ELISA, WB, IF, FC
Species Reactivity: Human, Mouse, Rat
-
Phospho-YAP1 (S127) Recombinant Monoclonal Antibody
Applications: ELISA, WB, IHC
Species Reactivity: Human
-
-
-
-
-