The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
追加情報ELISA: 1/10000 - 1/100000.
IHC-FoFr: 1/100 (PMID 19279043).
WB: 1/1000 - 1/5000. Detects a band of approximately 27 kDa.
Not yet tested in other applications.
Optimal dilutions/concentrations should be determined by the end user.
機能Functions in mitochondrial tRNA maturation. Part of mitochondrial ribonuclease P, an enzyme composed of MRPP1/RG9MTD1, MRPP2/HSD17B10 and MRPP3/KIAA0391, which cleaves tRNA molecules in their 5'-ends. By interacting with intracellular amyloid-beta, it may contribute to the neuronal dysfunction associated with Alzheimer disease (AD).
組織特異性Expressed in normal tissues but is overexpressed in neurons affected in AD.
関連疾患Defects in HSD17B10 are the cause of 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency (MHBD deficiency) [MIM:300438]. MHBD deficiency leads to neurological abnormalities, including psychomotor retardation, and, in virtually all patients, loss of mental and motor skills. Defects in HSD17B10 are the cause of mental retardation syndromic X-linked type 10 (MRXS10) [MIM:300220]. MRXS10 is characterized by mild mental retardation, choreoathetosis and abnormal behavior. A chromosomal microduplication involving HSD17B10 and HUWE1 is the cause of mental retardation X-linked type 17 (MRX17) [MIM:300705]; also known as mental retardation X-linked type 31 (MRX31). Mental retardation is characterized by significantly sub-average general intellectual functioning associated with impairments in adaptative behavior and manifested during the developmental period. In contrast to syndromic or specific X-linked mental retardation which also present with associated physical, neurological and/or psychiatric manifestations, intellectual deficiency is the only primary symptom of non-syndromic X-linked mental retardation.
配列類似性Belongs to the short-chain dehydrogenases/reductases (SDR) family.
Mitochondrial L3 Hydroxyacyl CoA Dehydrogenase antibody
Mitochondrial ribonuclease P protein 2 antibody
Mitochondrial RNase P protein 2 antibody
Short chain dehydrogenase/reductase family 5C member 1 antibody
Short chain L 3 hydroxyacyl CoA dehydrogenase type 2 antibody
Short chain type dehydrogenase/reductase XH98G2 antibody
Short-chain type dehydrogenase/reductase XH98G2 antibody
Type 10 17b HSD antibody
Type 10 17beta hydroxysteroid dehydrogenase antibody
Type II HADH antibody
Anti-ERAB antibody (ab17297) 使用論文
This product has been referenced in:
Yu Y et al. Evaluation of blastomere biopsy using mouse model indicates the potential high-risk of neurodegenerative disorders in the offspring. Mol Cell Proteomics : (2009).
Read more (PubMed: 19279043) »