Thermo Fisher Scientific PRODH Polyclonal Antibody
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
PA554187 | - | Thermo Fisher Scientific PA554187 PRODH Polyclonal Antibody 100 ul pk | 재고문의 | pk | 776,000원 | - | 853,600원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Immunohistochemistry (Paraffin) (IHC (P))
1:50-1:200
Product Specifications
Species Reactivity
Human
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Recombinant protein corresponding to Human PRODH. Recombinant protein control fragment (Product #RP-92348). if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
PRODH,
uniProtId:
O43272-4,
ncbiNodeId:
9606,
antigenRange:
283-387,
antigenLength:
600,
antigenImageFileName:
PA5-54187_PRODH_O43272-4_Rabbit.svg,
antigenImageFileNamePDP:
PA5-54187_PRODH_O43272-4_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
0.1 mg/mL
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_2645954
Product Specific Information
Immunogen sequence: QESVAKLGIA SRAEIEDWFT AETLGVSGTM DLLDWSSLID SRTKLSKHLV VPNAQTGQLE PLLSRFTEEE ELQMTRMLQR MDVLAKKATE MGVRLMVDAE QTYFQ
Highest antigen sequence identity to the following orthologs: Mouse - 85%, Rat - 83%.
Target Information
The protein encoded by this gene is a mitochondrial proline dehydrogenase that catalyzes the first step in proline degradation. Defects in this gene are a cause of hyperprolinemia type 1 and possibly susceptibility to schizophrenia 4 (SCZD4). The gene is located on chromosome 22q11.21, a region which has also been associated with the contiguous gene deletion syndromes DiGeorge syndrome and CATCH22 syndrome.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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