Thermo Fisher Scientific Spastin Monoclonal Antibody (Sp 3G11-1)
상품 옵션 정보 | ||||||||
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
6683-MSM1-P1 | - | Thermo Fisher Scientific 6683-MSM1-P1 Spastin Monoclonal Antibody (Sp 3G11-1) 100 ug pk | 재고문의 | pk | 903,000원 | - | 993,300원 | |
6683-MSM1-P0 | - | Thermo Fisher Scientific 6683-MSM1-P0 Spastin Monoclonal Antibody (Sp 3G11-1) 20 ug pk | 재고문의 | pk | 451,000원 | - | 496,100원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
1-2 µg/mL
Immunohistochemistry (PFA fixed) (IHC (PFA))
1-2 µg/mL
Immunocytochemistry (ICC/IF)
1-2 µg/mL
ELISA (ELISA)
Assay-dependent
Product Specifications
Species Reactivity
Human, Mouse, Rat
Host/Isotype
Mouse / IgG2a, kappa
Class
Monoclonal
Type
Antibody
Clone
Sp 3G11-1
Immunogen
Recombinant full-length human Spastin protein. if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
Spastin,
uniProtId:
Q9UBP0-1,
ncbiNodeId:
9606,
antigenRange:
1-616,
antigenLength:
616,
antigenImageFileName:
6683-MSM1-P0_Spastin_Q9UBP0-1_House_mouse.svg,
antigenImageFileNamePDP:
6683-MSM1-P0_Spastin_Q9UBP0-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
200 µg/mL
Purification
Protein A/G
Storage buffer
PBS, pH 7.4, with 0.05% BSA
Contains
0.05% sodium azide
Storage conditions
4° C, do not freeze
Shipping conditions
Ambient (domestic); Wet ice (international)
Target Information
This gene encodes a member of the AAA (ATPases associated with a variety of cellular activities) protein family. Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis. The encoded ATPase may be involved in the assembly or function of nuclear protein complexes. Two transcript variants encoding distinct isoforms have been identified for this gene. Other alternative splice variants have been described but their full length sequences have not been determined. Mutations associated with this gene cause the most frequent form of autosomal dominant spastic paraplegia 4.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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