Thermo Fisher Scientific TIA1 (T-Cell-Restricted Intracellular Antigen-1) Recombinant Rabbit Monoclonal Antibody (TIA1/1352R)
상품 옵션 정보 | ||||||||
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
7072-RBM2-P0 | - | Thermo Fisher Scientific 7072-RBM2-P0 TIA1 (T-Cell-Restricted Intracellular Antigen-1) Recombinant Rabbit Monoclonal Antibody (TIA1/1352R) 20 ug pk | 재고문의 | pk | 0원 | - | 0원 | |
7072-RBM2-P1 | - | Thermo Fisher Scientific 7072-RBM2-P1 TIA1 (T-Cell-Restricted Intracellular Antigen-1) Recombinant Rabbit Monoclonal Antibody (TIA1/1352R) 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
Human
Host/Isotype
Rabbit / IgG, kappa
Expression System
HEK293 cells
Class
Recombinant Monoclonal
Type
Antibody
Clone
TIA1/1352R
Immunogen
Human bone marrow malignant cells from a non B, non T acute leukemia if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
TIA-1,
uniProtId:
P31483-1,
ncbiNodeId:
9606,
antigenRange:
1-386,
antigenLength:
386,
antigenImageFileName:
7072-RBM2-P0_TIA-1_P31483-1_Rabbit.svg,
antigenImageFileNamePDP:
7072-RBM2-P0_TIA-1_P31483-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $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
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
Noggin is involved in numerous developmental processes, such as neural tube fusion and joint formation. The morphogenesis of organs is initiated by a downgrowth from a layer of epithelial stem cells. This process is achieved through the receipt of signals from 1) a WNT protein (WNT3A) to stabilize beta-catenin; and 2) Noggin, which is a bone morphogenetic protein inhibitor. Noggin mutations in unrelated families with proximal symphalangism (SYM1) and multiple synostoses syndrome (SYNS1) have been identified, which have multiple joint fusion as their principal defect.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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