Anti-ERAB/HSD17B10 antibody
| 英文名称 | ERAB/HSD17B10 |
| 中文名称 | 内质网Aβ相关结合蛋白抗体 |
| 别 名 | HSD17B10; Mitochondrial L3 HydroJNCacyl CoA Dehydrogenase; 17 beta hydroJNCsteroid dehydrogenase 10; 17 beta hydroJNCsteroid dehydrogenase type 10; 17b HSD10; 3 hydroJNC 2 methylbutyryl CoA dehydrogenase; 3 hydroJNCacyl CoA dehydrogenase type 2; 3 hydroJNCacyl CoA dehydrogenase type II; AB binding alcohol dehydrogenase; ABAD; Ads9; Amyloid beta binding polypeptide; Amyloid beta peptide binding alcohol dehydrogenase; Amyloid beta peptide binding protein; CAMR; DUPXp11.22; Endoplasmic Reticulum Amyloid Binding Protein; Endoplasmic reticulum associated amyloid beta peptide binding protein; ER associated amyloid beta-binding protein; ERAB; HADH 2; HADH2; HCD 2; HCD2; HSD17B10; HydroJNCacyl CoA Dehydrogenase type II; HydroJNCacyl Coenzyme A dehydrogenase type II; HydroJNCsteroid (17 beta) dehydrogenase 10; Mental retardation X linked syndromic 11; MHBD; Mitochondrial L3 HydroJNCacyl CoA Dehydrogenase; Mitochondrial ribonuclease P protein 2; Mitochondrial RNase P protein 2; MRPP2; MRX17; SCHAD; SDR5C1; Short chain dehydrogenase/reductase family 5C member 1; Short chain L 3 hydroJNCacyl CoA dehydrogenase type 2; Short chain type dehydrogenase/reductase XH98G2; Type 10 17b HSD; Type 10 17beta hydroJNCsteroid dehydrogenase; Type II HADH; XH98G2. |
DATASHEET
Host:Mouse
Target Protein:ERAB/HSD17B10
IR:Immunogen Range:51-130/196
Clonality:Polyclonal
Isotype:IgG
Entrez Gene:3028
Swiss Prot:Q99714
Source:KLH conjugated synthetic peptide derived from human ERAB:51-130/196
Purification:affinity purified by Protein A
Storage:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
Background:This gene encodes 3-hydroJNCacyl-CoA dehydrogenase type II, a member of the short-chain dehydrogenase/reductase superfamily. The gene product is a mitochondrial protein that catalyzes the oxidation of a wide variety of fatty acids, alcohols, and steroids. The protein has been implicated in the development of Alzheimer's disease, and mutations in the gene are the cause of 2-methyl-3-hydroJNCbutyryl-CoA dehydrogenase deficiency (MHBD). Several alternatively spliced transcript variants have been identified, but the full-length nature of only two transcript variants has been determined. [provided by RefSeq, Jul 2008].
Size:100ul
Concentration:1mg/ml
Applications:ELISA(1:5000-10000)
IHC-P(1:100-500)
IHC-F(1:100-500)
IF(1:100-500)
Cross Reactive Species:Human
Mouse
Rat
Dog
Pig
Cow
Horse
Sheep
Guinea Pig
.
For research use only. Not intended for diagnostic or therapeutic use.
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