Thermo Fisher Scientific SPG7 Monoclonal Antibody (OTI1C12), TrueMAB
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
CF504420 | - | Thermo Fisher Scientific CF504420 SPG7 Monoclonal Antibody (OTI1C12), TrueMAB 100 ug pk | 재고문의 | pk | 786,000원 | - | 864,600원 |
Applications
Tested Dilution
Publications
Western Blot (WB)
1:500-1:2,000
Immunocytochemistry (ICC/IF)
1:50-1:100
Flow Cytometry (Flow)
1:100
Product Specifications
Species Reactivity
Human, Mouse
Host/Isotype
Mouse / IgG2a
Class
Monoclonal
Type
Antibody
Clone
OTI1C12
Immunogen
Human recombinant protein fragment corresponding to amino acids 300-573 of human SPG7 prodduced in E.coli. if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
SPG7,
uniProtId:
Q9UQ90-1,
ncbiNodeId:
9606,
antigenRange:
300-573,
antigenLength:
795,
antigenImageFileName:
CF504420_SPG7_Q9UQ90-1_House_mouse.svg,
antigenImageFileNamePDP:
CF504420_SPG7_Q9UQ90-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Lyophilized
Concentration
1 mg/mL
Purification
Affinity chromatography
Storage buffer
PBS, pH 7.3, with 8% trehalose
Contains
no preservative
Storage conditions
-20° C, Avoid Freeze/Thaw Cycles
Shipping conditions
Ambient (domestic); Wet ice (international)
Product Specific Information
For reconstitution, we recommend adding 100 µL distilled water to a final antibody concentration of about 1 mg/mL. To use this carrier-free antibody for conjugation experiments, we strongly recommend performing another round of desalting. (Zeba Spin Desalting Columns, 7KMWCO, 0.5 mL, Product # 89882)
Target Information
This gene encodes a mitochondrial metalloprotease protein that is a member of the AAA 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. Mutations in this gene cause autosomal recessive spastic paraplegia 7. Two transcript variants encoding distinct isoforms have been identified.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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