Thermo Fisher Scientific TTF-1/NKX2.1 (Thyroid and Lung Epithelial Marker) Recombinant Rabbit Monoclonal Antibody (TTF1/8143R)
상품 옵션 정보 | ||||||||
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
7080-RBM13-P0 | - | Thermo Fisher Scientific 7080-RBM13-P0 TTF-1/NKX2.1 (Thyroid and Lung Epithelial Marker) Recombinant Rabbit Monoclonal Antibody (TTF1/8143R pk | 재고문의 | pk | 0원 | - | 0원 | |
7080-RBM13-P1 | - | Thermo Fisher Scientific 7080-RBM13-P1 TTF-1/NKX2.1 (Thyroid and Lung Epithelial Marker) Recombinant Rabbit Monoclonal Antibody (TTF1/8143R pk | 재고문의 | pk | 0원 | - | 0원 |
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
Dog, Human
Host/Isotype
Rabbit / IgG, kappa
Expression System
CHO cells
Class
Recombinant Monoclonal
Type
Antibody
Clone
TTF1/8143R
Immunogen
Recombinant full-length human NXK2-1 (TTF-1) protein if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
Nkx2.1,
uniProtId:
P43699-1,
ncbiNodeId:
9606,
antigenRange:
1-371,
antigenLength:
371,
antigenImageFileName:
7080-RBM13-P0_Nkx2.1_P43699-1_Rabbit.svg,
antigenImageFileNamePDP:
7080-RBM13-P0_Nkx2.1_P43699-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
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
This gene encodes a protein initially identified as a thyroid-specific transcription factor. The encoded protein binds to thyroglobulin promoter and regulates the expression of thyroid-specific genes but has also been shown to regulate the expression of genes involved in morphogenesis. Mutations and deletions in this gene are associated with benign hereditary chorea, choreoathetosis, congenital hypothyroidism, and neonatal respiratory distress, and may be associated with thyroid cancer. Multiple transcript variants encoding different isoforms have been found for this gene.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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