Thermo Fisher Scientific STK32A Monoclonal Antibody (3B3)
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
H00202374-M04 | - | Thermo Fisher Scientific H00202374-M04 STK32A Monoclonal Antibody (3B3) 100 ug pk | 재고문의 | pk | 520,000원 | - | 572,000원 |
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Applications
Tested Dilution
Publications
ELISA (ELISA)
10 µg/mL
Product Specifications
Species Reactivity
Human
Host/Isotype
Mouse / IgG2a, kappa
Class
Monoclonal
Type
Antibody
Clone
3B3
Immunogen
STK32A (AAH21666, 67 a.a. approximately 166 a.a) partial 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 = \[{
targetFamily:
STK32A,
uniProtId:
Q8WU08-1,
ncbiNodeId:
9606,
antigenRange:
67-166,
antigenLength:
396,
antigenImageFileName:
H00202374-M04_STK32A_Q8WU08-1_House_mouse.svg,
antigenImageFileNamePDP:
H00202374-M04_STK32A_Q8WU08-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $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: NVFKELQIMQ GLEHPFLVNL WYSFQDEEDM FMVVDLLLGG DLRYHLQQNV HFKEETVKLF ICELVMALDY LQNQRIIHRD MKPDNILLDE HDTWLSYKSH
Target Information
STK32A (serine/threonine kinase 32A), also known as YANK1, is a 396 amino acid protein that belongs to the superfamily of serine/threonine protein kinases and exists as three isoforms. The gene encoding STK32A maps to human chromosome 5, which is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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