Thermo Fisher Scientific RAB40B Monoclonal Antibody (1A1)
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
H00010966-M01A | - | Thermo Fisher Scientific H00010966-M01A RAB40B Monoclonal Antibody (1A1) 200 ul pk | 재고문의 | pk | 520,000원 | - | 572,000원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
ELISA (ELISA)
10 µg/mL
Product Specifications
Species Reactivity
Human
Host/Isotype
Mouse / IgG1, kappa
Class
Monoclonal
Type
Antibody
Clone
1A1
Immunogen
RAB40B (AAH18039, 179 a.a. approximately 278 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 = \[{
targetFamily:
RAB40B,
uniProtId:
Q12829-1,
ncbiNodeId:
9606,
antigenRange:
179-278,
antigenLength:
278,
antigenImageFileName:
H00010966-M01A_RAB40B_Q12829-1_House_mouse.svg,
antigenImageFileNamePDP:
H00010966-M01A_RAB40B_Q12829-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
See Label
Storage buffer
ascites
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: GMDRLWRPSK VLSLQDLCCR AVVSCTPVHL VDKLPLPIAL RSHLKSFSMA NGLNARMMHG GSYSLTTSST HKRSSLRKVK LVRPPQSPPK NCTRNSCKIS
Target Information
Rab 40B is a 278 amino acid protein that belongs to the small GTPase superfamily and the Rab family. Rab 40B contains a SOCS box domain that mediates interactions with the Elongin BC complex, an adapter module in different E3 ubiquitin ligase complexes. Rab 40B shares similarity with a yeast protein, suggesting a role in regulation of secretory vesicles. The Rab 40B gene is conserved in chimpanzee, cow, mouse, rat, chicken and zebrafish, and maps to human chromosome 17q25.3. It has been suggested that there is a major gene locus on chromosome 17q25.3 for autosomal dominant moyamoya disease (MMD), which is an idiopathic steno-occlusive cerebrovascular disease that represents an important cause of stroke.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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