Human HSD17B4 ELISA Kit (V2LY-0626-LY5012)

Go to compare Compare Online Inquiry
Tested Data
Request for COA
Datasheet Target References Q & As Review & reward Protocols Associated Products

Basic Information

Sensitivity
0.0041 ng/mL
Detection Range
0.01-2 ng/mL
Sample Type
Serum, Plasma, cell culture supernates
Specificity
Human
Assay Type
Sandwich
Reactivity
Human
Assay Time
1.5 h
Molecule Mass
79.7 kDa
Components
  • Pre-coated ELISA Plate: 12 wells * 8 detachable strips
  • Standard solution: 0.5ml x1
  • Standard diluent: 3ml x1
  • Streptavidin-HRP: 6ml x1
  • Stop solution: 6ml x1
  • Substrate solution A: 6ml x1
  • Substrate solution B: 6ml x1
  • Wash buffer concentrate (25x): 20ml x1
  • Biotinylated antibody: 1ml x1

Formulations & Storage [For reference only, actual COA shall prevail!]

Storage
Store at 2-8°C
More Infomation

Target

Full Name
hydroxysteroid (17-beta) dehydrogenase 4
Function
Bifunctional enzyme acting on the peroxisomal beta-oxidation pathway for fatty acids. Catalyzes the formation of 3-ketoacyl-CoA intermediates from straight-chain, 2-methyl-branched-chain fatty acids bile acid intermediates. With EHHADH, catalyzes the hydration of trans-2-enoyl-CoA and the dehydrogenation of 3-hydroxyacyl-CoA, but with opposite chiral specificity (PubMed:10671535).
Biological Process
Androgen metabolic process Source: UniProtKB
Estrogen metabolic process Source: UniProtKB
Fatty acid beta-oxidation Source: UniProtKB
Medium-chain fatty-acyl-CoA metabolic process Source: UniProtKB
Osteoblast differentiation Source: UniProtKB
Sertoli cell development Source: Ensembl
Very long-chain fatty acid metabolic process Source: Ensembl
Very long-chain fatty-acyl-CoA metabolic process Source: UniProtKB
Cellular Location
Peroxisome
Involvement in disease
D-bifunctional protein deficiency (DBPD):
Disorder of peroxisomal fatty acid beta-oxidation.
Perrault syndrome 1 (PRLTS1):
A sex-influenced disorder characterized by sensorineural deafness in both males and females and ovarian dysgenesis in females. Some patients also have neurologic manifestations, including mild mental retardation and cerebellar and peripheral nervous system involvement.

Arai, N., Hattori, N., Yamashita, S., Liu, Y. Y., Ebata, T., Takeuchi, C., ... & Ushijima, T. (2023). HSD17B4 methylation enhances glucose dependence of BT-474 breast cancer cells and increases lapatinib sensitivity. Breast Cancer Research and Treatment, 1-12.

Chen, S., Du, L., Lei, Y., Lin, Y., Chen, S., & Liu, Y. (2021). Two novel HSD17B4 heterozygous mutations in association with D-Bifunctional protein deficiency: a case report and literature review. Frontiers in Pediatrics, 9, 679597.

Lee, S. A., Lee, J., Kim, K., Moon, H., Min, C., Moon, B., ... & Park, D. (2021). The peroxisomal localization of Hsd17b4 is regulated by its interaction with phosphatidylserine. Molecules and Cells, 44(4), 214.

Yamashita, S., Hattori, N., Fujii, S., Yamaguchi, T., Takahashi, M., Hozumi, Y., ... & Mukai, H. (2020). Multi-omics analyses identify HSD17B4 methylation-silencing as a predictive and response marker of HER2-positive breast cancer to HER2-directed therapy. Scientific Reports, 10(1), 15530.

Huang, H., Liu, R., Huang, Y., Feng, Y., Fu, Y., Chen, L., ... & Chen, Y. (2020). Acetylation-mediated degradation of HSD17B4 regulates the progression of prostate cancer. Aging (Albany NY), 12(14), 14699.

Zhang, X., Yang, H., Zhang, J., Gao, F., & Dai, L. (2020). HSD17B4, ACAA1, and PXMP4 in peroxisome pathway are down-regulated and have clinical significance in non-small cell lung cancer. Frontiers in Genetics, 11, 273.

Matsuda, Y., Morino, H., Miyamoto, R., Kurashige, T., Kume, K., Mizuno, N., ... & Kawakami, H. (2020). Biallelic mutation of HSD17B4 induces middle age–onset spinocerebellar ataxia. Neurology Genetics, 6(1).

Violante, S., Achetib, N., van Roermund, C. W., Hagen, J., Dodatko, T., Vaz, F. M., ... & Houten, S. M. (2019). Peroxisomes can oxidize medium-and long-chain fatty acids through a pathway involving ABCD3 and HSD17B4. The FASEB Journal, 33(3), 4355.

Pan, L. C., Xiao, H. Y., Yin, W. J., & Lin, Z. (2018). Correlation between HSD17B4 expression in rat liver cancer tissues and inflammation or proliferation. Eur Rev Med Pharmacol Sci, 22(11), 3386-3393.

Ko, H. K., Berk, M., Chung, Y. M., Willard, B., Bareja, R., Rubin, M., ... & Sharifi, N. (2018). Loss of an androgen-inactivating and isoform-specific HSD17B4 splice form enables emergence of castration-resistant prostate cancer. Cell reports, 22(3), 809-819.

Ask a question We look forward to hearing from you.
0 reviews or Q&As
Loading...
Have you used Human HSD17B4 ELISA Kit?
Submit a review and get a Coupon or an Amazon gift card. 20% off Coupon $30 eGift Card
Submit a review
Loading...
For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

Online Inquiry

Contact us

  • Tel: (USA)
  • (UK)
  • Fax:
  • Email:

Submit A Review

online inquiry
Online Inquiry

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.