Thermo Fisher Scientific ATP7B Polyclonal Antibody, DyLight 650
상품 옵션 정보 | ||||||||
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
PA522768 | - | Thermo Fisher Scientific PA522768 ATP7B Polyclonal Antibody, DyLight 650 100 ul pk | 재고문의 | pk | 724,000원 | - | 796,400원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
1:1,000
Immunocytochemistry (ICC/IF)
1:10-1:2,000
Product Specifications
Species Reactivity
Human, Rat
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
A synthetic peptide made to an internal sequence nearer the C-terminus of human ATP7b. if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
ATP7B,
uniProtId:
P35670-1,
ncbiNodeId:
9606,
antigenRange:
1465,
antigenLength:
1465,
antigenImageFileName:
PA5-22768_ATP7B_P35670-1_Rabbit.svg,
antigenImageFileNamePDP:
PA5-22768_ATP7B_P35670-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
DyLight™ 650 DyLight™ 650 DyLight™ 650
Excitation/Emission Max
651/673 nm View spectra
Form
Liquid
Concentration
0.76 mg/mL
Purification
Antigen affinity chromatography
Storage buffer
50mM sodium borate
Contains
0.05% sodium azide
Storage conditions
4° C, store in dark
Shipping conditions
Ambient (domestic); Wet ice (international)
RRID
AB_11157445
Product Specific Information
This antibody does not react with mouse samples.
Target Information
This gene is a member of the P-type cation transport ATPase family and encodes a protein with several membrane-spanning domains, an ATPase consensus sequence, a hinge domain, a phosphorylation site, and at least 2 putative copper-binding sites. This protein functions as a monomer, exporting copper out of the cells, such as the efflux of hepatic copper into the bile. Alternate transcriptional splice variants, encoding different isoforms with distinct cellular localizations, have been characterized. Mutations in this gene have been associated with Wilson disease (WD).
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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