Thermo Fisher Scientific SOD1 Recombinant Rabbit Monoclonal Antibody (JF1005)
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
MA541208 | - | Thermo Fisher Scientific MA541208 SOD1 Recombinant Rabbit Monoclonal Antibody (JF1005) 100 ul pk | 재고문의 | pk | 724,000원 | - | 796,400원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
1:1,000-1:2,000
Immunohistochemistry (Paraffin) (IHC (P))
1:1000-1:2000
Immunocytochemistry (ICC/IF)
1:50-1:200
Flow Cytometry (Flow)
1:50-1:100
Product Specifications
Species Reactivity
Human, Rat
Host/Isotype
Rabbit / IgG
Expression System
HEK293 cells
Class
Recombinant Monoclonal
Type
Antibody
Clone
JF1005
Immunogen
Synthetic peptide within human superoxide dismutase 1 aa 105-154 / 154. if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
SOD1,
uniProtId:
P00441-1,
ncbiNodeId:
9606,
antigenRange:
105-154,
antigenLength:
154,
antigenImageFileName:
MA5-41208_SOD1_P00441-1_Rabbit.svg,
antigenImageFileNamePDP:
MA5-41208_SOD1_P00441-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
1 mg/mL
Purification
Protein A
Storage buffer
TBS, pH 7.4, with 40% glycerol, 0.05% BSA
Contains
0.05% sodium azide
Storage conditions
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping conditions
Wet ice
RRID
AB_2898962
Target Information
SOD1 (superoxide dismutase) binds copper and zinc ions and is one of two isozymes responsible for destroying free superoxide radicals in the body. This isozyme is a soluble cytoplasmic protein, acting as a homodimer to convert naturally-occuring but harmful superoxide radicals to molecular oxygen and hydrogen peroxide. The other isozyme is a mitochondrial protein. Mutations in this gene have been implicated as causes of familial amyotrophic lateral sclerosis. Rare transcript variants have been reported for this gene.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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