Thermo Fisher Scientific TWIST1 Monoclonal Antibody (10E4E6)
상품 옵션 정보 | ||||||||
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
MA538652 | - | Thermo Fisher Scientific MA538652 TWIST1 Monoclonal Antibody (10E4E6) 100 ug pk | 재고문의 | pk | 698,000원 | - | 767,800원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
1:500-1:2,000
Immunohistochemistry (Paraffin) (IHC (P))
1:200-1:1,000
Immunocytochemistry (ICC/IF)
1:200-1:1,000
Flow Cytometry (Flow)
1:200-1:400
ELISA (ELISA)
1:10,000
Product Specifications
Species Reactivity
Human, Mouse
Host/Isotype
Mouse / IgG1
Class
Monoclonal
Type
Antibody
Clone
10E4E6
Immunogen
Purified recombinant fragment of human TWIST1 (aa: 9-74) expressed in E. Coli. if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
TWIST1,
uniProtId:
Q15672-1,
ncbiNodeId:
9606,
antigenRange:
9-74,
antigenLength:
202,
antigenImageFileName:
MA5-38652_TWIST1_Q15672-1_House_mouse.svg,
antigenImageFileNamePDP:
MA5-38652_TWIST1_Q15672-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
1 mg/mL
Purification
Protein G
Storage buffer
PBS
Contains
0.05% sodium azide
Storage conditions
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping conditions
Ambient (domestic); Wet ice (international)
RRID
AB_2898564
Product Specific Information
This antibody has been tested in indirect ELISA.
Target Information
TWIST1 acts as a transcriptional regulator. It inhibits myogensis by sequestering E proteins, inhibiting trans-activation by MEF2, and inhibiting DNA-binding by MYOD1 through physical interaction. TWIST1 also represses proinflammatory cytokines such as TNFA and IL1B. TWIST also regulates cranial suture patterning and fusion and gene expression differentially depending on dimer composition. Mutations in the gene are implicated in Saethre-Chotzen syndrome, a disease characterized by coronal synostosis, brachycephaly, low front hairline, facial asymmetry, hypertelorism, broad halluces, and clinodactyly.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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