Thermo Fisher Scientific HSD17B4/MFE-2/17-beta-HSD4 Polyclonal Antibody
상품 옵션 정보 | ||||||||
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
A304797A | - | Thermo Fisher Scientific A304797A HSD17B4/MFE-2/17-beta-HSD4 Polyclonal Antibody 100 ul pk | 재고문의 | pk | 661,000원 | - | 727,100원 | |
A304797AT | - | Thermo Fisher Scientific A304797AT HSD17B4/MFE-2/17-beta-HSD4 Polyclonal Antibody 10 ul pk | 재고문의 | pk | 195,000원 | - | 214,500원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
Assay-dependent
Immunoprecipitation (IP)
2-10 µg/mg lysate
Product Specifications
Species Reactivity
Human
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Region between residue 600 to 650 of human Hydroxysteroid (17-Beta) Dehydrogenase 4. if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
HSD17B4,
uniProtId:
P51659-1,
ncbiNodeId:
9606,
antigenRange:
600-650,
antigenLength:
736,
antigenImageFileName:
A304-797A_HSD17B4_P51659-1_Rabbit.svg,
antigenImageFileNamePDP:
A304-797A_HSD17B4_P51659-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
1 mg/mL
Purification
Antigen affinity chromatography
Storage buffer
phosphate/tris citrate, pH 7-8
Contains
0.09% sodium azide
Storage conditions
4° C
Shipping conditions
Wet ice
Product Specific Information
The recommended shelf life for this product is 1 year from date of receipt.
Target Information
Peroxisomal multifunctional enzyme type 2 is a protein that in humans is encoded by the HSD17B4 gene. The protein encoded by this gene is a bifunctional enzyme that is involved in the peroxisomal beta-oxidation pathway for fatty acids. It also acts as a catalyst for the formation of 3-ketoacyl-CoA intermediates from both straight-chain and 2-methyl-branched-chain fatty acids. Defects in this gene that affect the peroxisomal fatty acid beta-oxidation activity are a cause of D-bifunctional protein deficiency (DBPD). An apparent pseudogene of this gene is present on chromosome 8. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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