Thermo Fisher Scientific AAAS Monoclonal Antibody (OTI7H7), TrueMAB
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
CF808617 | - | Thermo Fisher Scientific CF808617 AAAS Monoclonal Antibody (OTI7H7), TrueMAB 100 ug pk | 재고문의 | pk | 786,000원 | - | 864,600원 |
Applications
Tested Dilution
Publications
Western Blot (WB)
1:2,000
Immunohistochemistry (Paraffin) (IHC (P))
1:150
Product Specifications
Species Reactivity
Human, Mouse, Rat
Host/Isotype
Mouse / IgG2a
Class
Monoclonal
Type
Antibody
Clone
OTI7H7
Immunogen
Human recombinant protein fragment corresponding to amino acids 322-546 of human AAAS produced in E.coli. if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
Aladin,
uniProtId:
Q9NRG9-1,
ncbiNodeId:
9606,
antigenRange:
322-546,
antigenLength:
546,
antigenImageFileName:
CF808617_Aladin_Q9NRG9-1_House_mouse.svg,
antigenImageFileNamePDP:
CF808617_Aladin_Q9NRG9-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $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
The protein encoded by this gene is a member of the WD-repeat family of regulatory proteins and may be involved in normal development of the peripheral and central nervous system. The encoded protein is part of the nuclear pore complex and is anchored there by NDC1. Defects in this gene are a cause of achalasia-addisonianism-alacrima syndrome (AAAS), also called triple-A syndrome or Allgrove syndrome. Two transcript variants encoding different isoforms have been found for this gene.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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