Thermo Fisher Scientific GPR179 Polyclonal Antibody
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
PA553657 | - | Thermo Fisher Scientific PA553657 GPR179 Polyclonal Antibody 100 ul pk | 재고문의 | pk | 776,000원 | - | 853,600원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Immunohistochemistry (Paraffin) (IHC (P))
1:200-1:500
Product Specifications
Species Reactivity
Human
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Recombinant protein corresponding to Human GPR179. Recombinant protein control fragment (Product #RP-91290). if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
GPR179,
uniProtId:
Q6PRD1-1,
ncbiNodeId:
9606,
antigenRange:
109-253,
antigenLength:
2367,
antigenImageFileName:
PA5-53657_GPR179_Q6PRD1-1_Rabbit.svg,
antigenImageFileNamePDP:
PA5-53657_GPR179_Q6PRD1-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
0.4 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_2642176
Product Specific Information
Immunogen sequence: LNMLLQANDI RESSVEEDVE WYQALVRSVA EGDPRVYRAL LTFNPPPGAS HLQLALQATR TGEETILQDL SGNWVQEENP PGDLDTPALK KRVLTNDLGS LGSPKWPQAD GYVGDTQQVR LSPPFLECQE GRLRPGWLIT LSATF
Highest antigen sequence identity to the following orthologs: Mouse - 84%, Rat - 86%.
Target Information
Probable G-protein coupled receptor 179 is a protein that in humans is encoded by the GPR179 gene. This gene encodes a member of the glutamate receptor subfamily of G protein-coupled receptors. The encoded protein has an EGF-like calcium binding domain and a seven transmembrane domain in the N-terminal region of the protein. Mutations in this gene are associated with congenital stationary night blindness type 1E.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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