Thermo Fisher Scientific HSD17B4 Polyclonal Antibody
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
PA5110873 | - | Thermo Fisher Scientific PA5110873 HSD17B4 Polyclonal Antibody 100 ul pk | 재고문의 | pk | 775,000원 | - | 852,500원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
0.04-0.4 µg/mL
Immunohistochemistry (Paraffin) (IHC (P))
1:20-1:50
Product Specifications
Species Reactivity
Human
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Recombinant Protein corresonding to Human HSD17B4. Recombinant protein control fragment (Product #RP-93145). if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
HSD17B4,
uniProtId:
P51659-1,
ncbiNodeId:
9606,
antigenRange:
97-222,
antigenLength:
736,
antigenImageFileName:
PA5-110873_HSD17B4_P51659-1_Rabbit.svg,
antigenImageFileNamePDP:
PA5-110873_HSD17B4_P51659-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Purification
Antigen affinity chromatography
Storage buffer
PBS, pH 7.2, with 40% glycerol
Contains
0.02% sodium azide
Storage conditions
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping conditions
Wet ice
RRID
AB_2856284
Product Specific Information
Immunogen sequence: VNNAGILRDR SFARISDEDW DIIHRVHLRG SFQVTRAAWE HMKKQKYGRI IMTSSASGIY GNFGQANYSA AKLGLLGLAN SLAIEGRKSN IHCNTIAPNA GSRMTQTVMP EDLVEALKPE YVAPLV
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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