Thermo Fisher Scientific DNMT3B Monoclonal Antibody (7E5E9C1)
상품 옵션 정보 | ||||||||
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
MA538512 | - | Thermo Fisher Scientific MA538512 DNMT3B Monoclonal Antibody (7E5E9C1) 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
Flow Cytometry (Flow)
1:200-1:400
ELISA (ELISA)
1:10,000
Product Specifications
Species Reactivity
Human
Host/Isotype
Mouse / IgG1
Class
Monoclonal
Type
Antibody
Clone
7E5E9C1
Immunogen
Purified recombinant fragment of human DNMT3B (aa: 1-150) expressed in E. Coli. if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
DNMT3B,
uniProtId:
Q9UBC3-1,
ncbiNodeId:
9606,
antigenRange:
1-150,
antigenLength:
853,
antigenImageFileName:
MA5-38512_DNMT3B_Q9UBC3-1_House_mouse.svg,
antigenImageFileNamePDP:
MA5-38512_DNMT3B_Q9UBC3-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $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_2898425
Product Specific Information
This antibody has been tested in indirect ELISA.
Target Information
CpG methylation is an epigenetic modification that is important for embryonic development, imprinting, and X-chromosome inactivation. Studies in mice have demonstrated that DNA methylation is required for mammalian development. This gene encodes a DNA methyltransferase which is thought to function in de novo methylation, rather than maintenance methylation. The protein localizes primarily to the nucleus and its expression is developmentally regulated. Mutations in this gene cause the immunodeficiency-centromeric instability-facial anomalies (ICF) syndrome. Six alternatively spliced transcript variants have been described. The full length sequences of variants 4 and 5 have not been determined.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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