Thermo Fisher Scientific CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) Monoclonal Antibody (CFTR/1785)
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
1080-MSM10-P1 | - | Thermo Fisher Scientific 1080-MSM10-P1 CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) Monoclonal Antibody (CFTR/1785) 100 ug pk | 재고문의 | pk | 903,000원 | - | 993,300원 | |
1080-MSM10-P0 | - | Thermo Fisher Scientific 1080-MSM10-P0 CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) Monoclonal Antibody (CFTR/1785) 20 ug pk | 재고문의 | pk | 451,000원 | - | 496,100원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Immunohistochemistry (Paraffin) (IHC (P))
Assay-dependent
Immunohistochemistry (PFA fixed) (IHC (PFA))
1-2 µg/mL
Product Specifications
Species Reactivity
Human
Host/Isotype
Mouse / IgG2b, kappa
Class
Monoclonal
Type
Antibody
Clone
CFTR/1785
Immunogen
Recombinant fragment (around aa 258-385) of human CFTR protein. if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
CFTR,
uniProtId:
P13569-1,
ncbiNodeId:
9606,
antigenRange:
258-385,
antigenLength:
1480,
antigenImageFileName:
1080-MSM10-P0_CFTR_P13569-1_House_mouse.svg,
antigenImageFileNamePDP:
1080-MSM10-P0_CFTR_P13569-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
200 µg/mL
Purification
Protein A/G
Storage buffer
PBS, pH 7.4, with 0.05% BSA
Contains
0.05% sodium azide
Storage conditions
4° C, do not freeze
Shipping conditions
Ambient (domestic); Wet ice (international)
Target Information
Cystic Fibrosis (CF) is a common lethal genetic disease caused by mutations of the gene coding for the cystic fibrosis transmembrane conductance factor, a cAMP regulated chloride channel. Approximately 70% of all CF cases share the deletion of a phenylalanine at position 508 (delta F508) which results in abnormal chloride transport. Since the CF mutation is lethal, most often by lung and liver disease, it raises the question of why this genetic disease remains as common as it is. One possible explanation is that Salmonella typhi has been shown to use CFTR to enter intestinal epithelial cells and that delta F508 heterozygote and homozygote mice showed 86% and 100% reductions in S. typhi intestinal submucosal uptake.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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