Thermo Fisher Scientific G6PD Polyclonal Antibody
상품 옵션 정보 | ||||||||
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
IHC00007 | - | Thermo Fisher Scientific IHC00007 G6PD Polyclonal Antibody 100 ul pk | 재고문의 | pk | 700,000원 | - | 770,000원 | |
IHC00007T | - | Thermo Fisher Scientific IHC00007T G6PD Polyclonal Antibody 10 ul pk | 재고문의 | pk | 195,000원 | - | 214,500원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Immunohistochemistry (IHC)
1:100-1:500
Immunohistochemistry (Paraffin) (IHC (P))
1:100-1:500
Product Specifications
Species Reactivity
Human, Mouse
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Region between residue 50 and 100 of human Glucose-6-Phosphate Dehydrogenase. if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
G6PD,
uniProtId:
P11413-1,
ncbiNodeId:
9606,
antigenRange:
50-100,
antigenLength:
515,
antigenImageFileName:
IHC-00007_G6PD_P11413-1_Rabbit.svg,
antigenImageFileNamePDP:
IHC-00007_G6PD_P11413-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
0.25 mg/mL
Purification
Antigen affinity chromatography
Storage buffer
TBS, pH 7.0 to 8.0, with 0.1% BSA
Contains
0.09% sodium azide
Storage conditions
4° C
Shipping conditions
Wet ice
Product Specific Information
The recommended shelf life for this product is 1 year from date of receipt.
Based on 100% sequence identity, this antibody is predicted to react with Monkey, Gorilla, Chimpanzee, Northern white-cheeked gibbon, Olive baboon and Crab-eating macaque
Target Information
This gene encodes glucose-6-phosphate dehydrogenase. This protein is a cytosolic enzyme encoded by a housekeeping X-linked gene whose main function is to produce NADPH, a key electron donor in the defense against oxidizing agents and in reductive biosynthetic reactions. G6PD is remarkable for its genetic diversity. Many variants of G6PD, mostly produced from missense mutations, have been described with wide ranging levels of enzyme activity and associated clinical symptoms. G6PD deficiency may cause neonatal jaundice, acute hemolysis, or severe chronic non-spherocytic hemolytic anemia. 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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