Thermo Fisher Scientific NDUFS7 Monoclonal Antibody (3A3)
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
H00374291-M01 | - | Thermo Fisher Scientific H00374291-M01 NDUFS7 Monoclonal Antibody (3A3) 100 ug pk | 재고문의 | pk | 520,000원 | - | 572,000원 |
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Applications
Tested Dilution
Publications
ELISA (ELISA)
10 µg/mL
Product Specifications
Species Reactivity
Human
Host/Isotype
Mouse / IgG2b, kappa
Class
Monoclonal
Type
Antibody
Clone
3A3
Immunogen
NDUFS7 (NP_077718, 114 a.a. approximately 213 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa. if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
NDUFS7,
uniProtId:
O75251-1,
ncbiNodeId:
9606,
antigenRange:
114-213,
antigenLength:
213,
antigenImageFileName:
H00374291-M01_NDUFS7_O75251-1_House_mouse.svg,
antigenImageFileNamePDP:
H00374291-M01_NDUFS7_O75251-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
See Label
Purification
Affinity chromatography
Storage buffer
PBS, pH 7.4
Contains
no preservative
Storage conditions
-20° C, Avoid Freeze/Thaw Cycles
Shipping conditions
Ambient (domestic); Wet ice (international)
Product Specific Information
Sequence of this protein is as follows: PRQSDVMIVA GTLTNKMAPA LRKVYDQMPE PRYVVSMGSC ANGGGYYHYS YSVVRGCDRI VPVDIYIPGC PPTAEALLYG ILQLQRKIKR ERRLQIWYRR
Target Information
This gene encodes a protein that is a subunit of one of the complexes that forms the mitochondrial respiratory chain. This protein is one of over 40 subunits found in complex I, the nicotinamide adenine dinucleotide (NADH):ubiquinone oxidoreductase. This complex functions in the transfer of electrons from NADH to the respiratory chain, and ubiquinone is believed to be the immediate electron acceptor for the enzyme. Mutations in this gene cause Leigh syndrome due to mitochondrial complex I deficiency, a severe neurological disorder that results in bilaterally symmetrical necrotic lesions in subcortical brain regions.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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