Thermo Fisher Scientific GTF2I Monoclonal Antibody (2D6)
상품 옵션 정보 | ||||||||
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
H00002969-M02 | - | Thermo Fisher Scientific H00002969-M02 GTF2I Monoclonal Antibody (2D6) 100 ug pk | 재고문의 | pk | 520,000원 | - | 572,000원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
1-5 µg/mL
Immunocytochemistry (ICC/IF)
10 µg/mL
ELISA (ELISA)
0.1 ng/mL
Product Specifications
Species Reactivity
Human
Host/Isotype
Mouse / IgG2a, kappa
Class
Monoclonal
Type
Antibody
Clone
2D6
Immunogen
GTF2I (AAH04472.1, 36 a.a. approximately 274 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa. if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
GTF2I,
uniProtId:
P78347-1,
ncbiNodeId:
9606,
antigenRange:
1-998,
antigenLength:
998,
antigenImageFileName:
H00002969-M02_GTF2I_P78347-1_House_mouse.svg,
antigenImageFileNamePDP:
H00002969-M02_GTF2I_P78347-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
See Label
Purification
Affinity chromatography
Storage buffer
PBS, pH 7.4
Contains
no preservative
Storage conditions
-20° C, Avoid Freeze/Thaw Cycles
Shipping conditions
Ambient (domestic); Wet ice (international)
Product Specific Information
Sequence of this protein is as follows: ELAKSKAEVA CIAVYETDVF VVGTERGRAF VNTRKDFQKD FVKYCVEEEE KAAEMHKMKS TTQANRMSVD AVEIETLRKT VEDYFCFCYG KALGKSTVVP VPYEKMLRDQ SAVVVQGLPE GVAFKHPENY DLATLKWILE NKAGISFIIK RPFLEPKKHV GGRVMVTDAD RSILSPGGSC GPIKVKTEPT EDSGISLEMA AVTVKEESED PDYYQYNIQG SHHSSEGNEG TEMEVPAEG
Target Information
This gene encodes a multifunctional phosphoprotein with roles in transcription and signal transduction. It is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11. 23. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 7, 13 and 21.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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