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ELK Biotechnology 17β-HSD4 rabbit pAb
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ELK Biotechnology 17β-HSD4 rabbit pAb

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17β-HSD4 단백질을 인식하는 토끼 폴리클로날 항체로, WB, IHC, IF, ELISA에 적합합니다. 인간, 생쥐, 랫드에 반응하며 peroxisomal β-oxidation 연구에 유용합니다. 고순도 IgG 형식으로 -20°C에서 1년 보관 가능합니다.

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ELK Biotechnology ES4116-100UL 17β-HSD4 rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES4116-50UL 17β-HSD4 rabbit pAb, 50UL pk판매 단위 pk ·
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301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology 17β-HSD4 rabbit pAb

ELK Biotechnology 17β-HSD4 rabbit pAb

제품 정보

항목 내용
Product Name 17β-HSD4 rabbit pAb
Alternative Names HSD17B4; EDH17B4; Peroxisomal multifunctional enzyme type 2; MFE-2; 17-beta-hydroxysteroid dehydrogenase 4; 17-beta-HSD 4; D-bifunctional protein; DBP; Multifunctional protein 2; MPF-2
Applications WB; IHC; IF; ELISA
Recommended Dilutions WB: 1/500–1/2000; IHC-p: 1/100–1/300; ELISA: 1/20000; Other applications not yet tested
Immunogen Synthesized peptide derived from N-terminal region of human HSD17B4 (AA range: 41–90)
Host Rabbit
Storage -20°C / 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 80 kD
Gene ID (Human) 3295
Human Swiss-Prot No P51659
Cellular Localization Peroxisome
Species Reactivity Human; Mouse; Rat

Background

Hydroxysteroid 17-beta dehydrogenase 4 (HSD17B4) is a bifunctional enzyme involved in the peroxisomal β-oxidation pathway for fatty acids. It catalyzes the formation of 3-ketoacyl-CoA intermediates from both straight-chain and 2-methyl-branched-chain fatty acids. Defects in this gene that impair peroxisomal fatty acid β-oxidation cause D-bifunctional protein deficiency (DBPD). A pseudogene of HSD17B4 is located on chromosome 8. Multiple alternatively spliced transcript variants encoding distinct isoforms have been identified.
[Provided by RefSeq, May 2014]

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