Thermo Fisher Scientific HSP60 Recombinant Rabbit Monoclonal Antibody (23GB2680)
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 재고 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
MA553492 | - | Thermo Fisher Scientific MA553492 HSP60 Recombinant Rabbit Monoclonal Antibody (23GB2680) 100 uL pk | 재고문의 | pk | 0원 | - | 0원 | ||
MA553493 | - | Thermo Fisher Scientific MA553493 HSP60 Recombinant Rabbit Monoclonal Antibody (23GB2680) 20 uL pk | 재고문의 | pk | 0원 | - | 0원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
1:1,000-1:5,000
Immunocytochemistry (ICC/IF)
1:1,000
Flow Cytometry (Flow)
1:2,000
Product Specifications
Species Reactivity
Human, Mouse, Rat
Host/Isotype
Rabbit / IgG
Expression System
HEK293F
Class
Recombinant Monoclonal
Type
Antibody
Clone
23GB2680
Immunogen
A synthesized peptide derived from human Hsc60 (420-460AA). if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
HSP60,
uniProtId:
P10809-1,
ncbiNodeId:
9606,
antigenRange:
420-460,
antigenLength:
573,
antigenImageFileName:
MA5-53492_HSP60_P10809-1_Rabbit.svg,
antigenImageFileNamePDP:
MA5-53492_HSP60_P10809-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Purification
Affinity chromatography
Storage buffer
PBS, pH 7.4, with 50% glycerol
Contains
0.02% sodium azide
Storage conditions
-20°C
Shipping conditions
Wet ice (domestic); Dry ice (international)
Target Information
This gene encodes a member of the chaperonin family. The encoded mitochondrial protein may function as a signaling molecule in the innate immune system. This protein is essential for the folding and assembly of newly imported proteins in the mitochondria. This gene is adjacent to a related family member and the region between the 2 genes functions as a bidirectional promoter. Several pseudogenes have been associated with this gene. Two transcript variants encoding the same protein have been identified for this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 13.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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