Thermo Fisher Scientific MCFD2 Monoclonal Antibody (294301)
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
MA524000 | - | Thermo Fisher Scientific MA524000 MCFD2 Monoclonal Antibody (294301) 100 ug pk | 재고문의 | pk | 537,000원 | - | 590,700원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
1 µg/mL
Immunohistochemistry (IHC)
8-25 µg/mL
Product Specifications
Species Reactivity
Human
Host/Isotype
Mouse / IgG2b
Class
Monoclonal
Type
Antibody
Clone
294301
Immunogen
E. coli-derived recombinant human SDNSF/MCFD2 Glu27-Gln146 if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
MCFD2,
uniProtId:
Q8NI22-1,
ncbiNodeId:
9606,
antigenRange:
27-146,
antigenLength:
146,
antigenImageFileName:
MA5-24000_MCFD2_Q8NI22-1_House_mouse.svg,
antigenImageFileNamePDP:
MA5-24000_MCFD2_Q8NI22-1_House_mouse_PDP.jpeg,
sortOrder:
2}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Lyophilized
Concentration
0.5 mg/mL
Purification
Protein A/G
Storage buffer
PBS with 5% trehalose
Contains
No Preservative
Storage conditions
-20° C, Avoid Freeze/Thaw Cycles
Shipping conditions
Ambient (domestic); Wet ice (international)
RRID
AB_2606510
Product Specific Information
In direct ELISAs, approximately 25% cross-reactivity with recombinant mouse SDNSF is observed. In Western blots, no cross-reactivity with recombinant mouse SDNSF is observed.
Reconstitute at 0.5 mg/mL in sterile PBS.
Target Information
Multiple coagulation factor deficiency protein 2 (MCFD2) is localized in the endoplasmic reticulum-Golgi intermediate compartment (ERGIC) through a direct, calcium-dependent interaction with LMAN1. The MCFD2-LMAN1 complex forms a specific cargo receptor for the transport of selected proteins from the endoplasmic reticulum to the Golgi apparatus. Mutations in the MCFD2 gene may cause of factor V and factor VIII combined deficiency (F5F8D). F5F8D is an autosomal recessive human bleeding disorder characterized by the reduction of both clotting proteins.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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