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Hydroxysteroid (17-Beta) Dehydrogenase 10 (HSD17B10) ELISA Kits

HSD17B10 encodes 3-hydroxyacyl-CoA dehydrogenase type II, a member of the short-chain dehydrogenase/reductase superfamily. Additionally we are shipping Hydroxysteroid (17-Beta) Dehydrogenase 10 Antibodies (108) and Hydroxysteroid (17-Beta) Dehydrogenase 10 Proteins (18) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
HSD17B10 3028 Q99714
HSD17B10 15108  
HSD17B10 63864 O70351
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Top Hydroxysteroid (17-Beta) Dehydrogenase 10 ELISA Kits at antibodies-online.com

Showing 5 out of 13 products:

Catalog No. Reactivity Sensitivity Range Images Quantity Supplier Delivery Price Details
Mouse 0.063 ng/mL 0.15-10 ng/mL 96 Tests Log in to see 9 to 11 Days
$757.89
Details
Human 6.25 pg/ml 25-1600 pg/mL   96 Tests Log in to see 11 to 13 Days
$910.56
Details
Human
  96 Tests Log in to see 2 to 3 Days
$350.00
Details
Rat
  96 Tests Log in to see 11 to 13 Days
$875.60
Details
Cow
  96 Tests Log in to see 11 to 13 Days
$1,029.60
Details

More ELISA Kits for Hydroxysteroid (17-Beta) Dehydrogenase 10 Interaction Partners

Human Hydroxysteroid (17-Beta) Dehydrogenase 10 (HSD17B10) interaction partners

  1. Data suggest that HSD10 plays a role in alterations of energy metabolism by regulating mtDNA content in colorectal carcinomas.

  2. upon exposure to E2, ERalpha (show ESR1 ELISA Kits) rapidly localizes to mitochondria, in which it interacts with HSD17B10 to modulate the expression of mitochondrial RNA transcripts.

  3. Our findings demonstrate that overexpression of HSD10 accelerates pheochromocytoma cell growth, enhances cell respiration, and increases cellular resistance to cell death induction.

  4. Three HSD10 variants associated with neurodegenerative disorders are inactive with cardiolipin

  5. The authors demonstrate elevated amounts of unprocessed pre-tRNAs and mRNA transcripts encoding mitochondrial subunits indicating deficient RNase P activity in HSD10 disease.

  6. The study showed that pathogenic mutations impair SDR5C1-dependent dehydrogenation, tRNA processing and methylation.

  7. loss of HSD10 causes impaired mitochondrial precursor transcript processing which may explain mitochondrial dysfunction observed in HSD10 disease

  8. Defects in this gene are a cause of 17beta-hydroxysteroid dehydrogenase (show HSD17B7 ELISA Kits) type 10 (HSD10) deficiency. The encoded protein does not exhibit generalized alcohol dehydrogenase (show AKR1A1 ELISA Kits) activity as was previously thought.

  9. Significantly higher levels of SRD5A1 (show SRD5A1 ELISA Kits), AKR1C2 (show AKR1C2 ELISA Kits), AKR1C3 (show AKR1C3 ELISA Kits), and HSD17B10 mRNA were however found in bone metastases than in non-malignant and/or malignant prostate tissue

  10. Inhibition of mitochondrial RNase P by beta-amyloid is an unspecific effect and is not mediated by beta-amyloid interaction with SDR5C1.

Mouse (Murine) Hydroxysteroid (17-Beta) Dehydrogenase 10 (HSD17B10) interaction partners

  1. that 17beta-HSD-10 is a major product of both fetal and adult-type Leydig cells.

  2. ABAD enhances Abeta (show APP ELISA Kits)-induced cell stress via mitochondrial dysfunction.Amyloid-beta peptide (Abeta (show APP ELISA Kits)) binding alcohol dehydrogenase (show AKR1A1 ELISA Kits) (ABAD), an enzyme present in neuronal mitochondria, is a cofactor facilitating Abeta (show APP ELISA Kits)-induced cell stress.

Hydroxysteroid (17-Beta) Dehydrogenase 10 (HSD17B10) Antigen Profile

Antigen Summary

This gene encodes 3-hydroxyacyl-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-hydroxybutyryl-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.

Gene names and symbols associated with HSD17B10

  • hydroxysteroid (17-beta) dehydrogenase 10 (HSD17B10) antibody
  • hydroxysteroid (17-beta) dehydrogenase 10 (hsd17b10) antibody
  • hydroxysteroid (17-beta) dehydrogenase 10 (LOC100342235) antibody
  • hydroxysteroid (17-beta) dehydrogenase 10 (Hsd17b10) antibody
  • 17b-HSD10 antibody
  • 17bHSD10 antibody
  • ABAD antibody
  • Ads9 antibody
  • CAMR antibody
  • DUPXp11.22 antibody
  • ERAB antibody
  • Hadh2 antibody
  • HCD2 antibody
  • hsd10 antibody
  • HSD17B10 antibody
  • im:6899159 antibody
  • MHBD antibody
  • MRPP2 antibody
  • MRX17 antibody
  • MRX31 antibody
  • MRXS10 antibody
  • SCHAD antibody
  • SDR5C1 antibody
  • wu:fj61f03 antibody
  • zgc:101605 antibody

Protein level used designations for HSD17B10

hydroxysteroid (17-beta) dehydrogenase 10 , 3-hydroxyacyl-CoA dehydrogenase type-2 , hydroxyacyl-Coenzyme A dehydrogenase, type II , 3-hydroxy-2-methylbutyryl-CoA dehydrogenase , AB-binding alcohol dehydrogenase , amyloid-beta peptide binding alcohol dehydrogenase , endoplasmic reticulum-associated amyloid beta-peptide-binding protein , mitochondrial RNase P subunit 2 , mitochondrial ribonuclease P protein 2 , short chain L-3-hydroxyacyl-CoA dehydrogenase type 2 , short chain dehydrogenase/reductase family 5C, member 1 , short chain type dehydrogenase/reductase XH98G2 , 17-beta-HSD 10 , 17-beta-hydroxysteroid dehydrogenase 10 , 3-hydroxyacyl-CoA dehydrogenase type II , hydroxyacyl-Coenzyme A dehydrogenase type II , mitochondrial RNase P protein 2 , type II HADH , amyloid beta-peptide binding protein , short chain L-3-hydroxyacyl-CoA dehydrogenase , hydroxyacyl-Coenzyme A dehydrogenase, type II hydroxyacyl-Coenzyme A

GENE ID SPECIES
425758 Gallus gallus
450078 Danio rerio
549265 Xenopus (Silurana) tropicalis
465649 Pan troglodytes
480930 Canis lupus familiaris
100342235 Oryctolagus cuniculus
3028 Homo sapiens
446903 Xenopus laevis
15108 Mus musculus
63864 Rattus norvegicus
281809 Bos taurus
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