Thermo Fisher Scientific XKR7 Polyclonal Antibody
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
PA559326 | - | Thermo Fisher Scientific PA559326 XKR7 Polyclonal Antibody 100 ul pk | 재고문의 | pk | 776,000원 | - | 853,600원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Immunohistochemistry (Paraffin) (IHC (P))
1:20-1:50
Product Specifications
Species Reactivity
Human
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Recombinant protein corresponding to Human XKR7. Recombinant protein control fragment (Product #RP-98368). if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
XKR7,
uniProtId:
Q5GH72-1,
ncbiNodeId:
9606,
antigenRange:
442-530,
antigenLength:
579,
antigenImageFileName:
PA5-59326_XKR7_Q5GH72-1_Rabbit.svg,
antigenImageFileNamePDP:
PA5-59326_XKR7_Q5GH72-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
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_2649688
Product Specific Information
Immunogen sequence: NGPMLGPQAP GCIFRKASEP CGPPADAITS PPRSLPRTTG AERDGASAGE RAGTPTPPVF QVRPGLPPTP VARTLRTEGP VIRIDLPRK
Highest antigen sequence identity to the following orthologs: Mouse - 89%, Rat - 91%.
Target Information
XKR7 (XK-related protein 7) is a 579 amino acid multi-pass membrane protein that likely is a component of the XK/Kell complex of the Kell blood group system. The gene encoding XKR7 maps to human chromosome 20, which comprises approximately 2% of the human genome. Chromosome 20 contains nearly 63 million bases that encode over 600 genes, some of which are associated with Creutzfeldt-Jakob disease, amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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