Thermo Fisher Scientific PGD Recombinant Rabbit Monoclonal Antibody (9A2M7)
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
MA542605 | - | Thermo Fisher Scientific MA542605 PGD Recombinant Rabbit Monoclonal Antibody (9A2M7) 100 ul pk | 재고문의 | pk | 786,000원 | - | 864,600원 |
Applications
Tested Dilution
Publications
Western Blot (WB)
1:500-1:1,000
Immunocytochemistry (ICC/IF)
1:50-1:200
ELISA (ELISA)
1 µg/mL
Immunoprecipitation (IP)
0.5 µg-4 µg antibody for 200 µg-400 µg extracts of
Product Specifications
Species Reactivity
Human, Mouse, Rat
Host/Isotype
Rabbit / IgG
Expression System
HEK293 cells
Class
Recombinant Monoclonal
Type
Antibody
Clone
9A2M7
Immunogen
A synthetic peptide corresponding to a sequence within amino acids 384-483 of human PGD (P52209). if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
PGD,
uniProtId:
P52209-1,
ncbiNodeId:
9606,
antigenRange:
384-483,
antigenLength:
483,
antigenImageFileName:
MA5-42605_PGD_P52209-1_Rabbit.svg,
antigenImageFileNamePDP:
MA5-42605_PGD_P52209-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
0.33 mg/mL
Purification
Affinity Chromatography
Storage buffer
PBS, pH 7.3, with 50% glycerol, 0.05% BSA
Contains
0.02% sodium azide
Storage conditions
-20° C, Avoid Freeze/Thaw Cycles
Shipping conditions
Ambient (domestic); Wet ice (international)
RRID
AB_2911746
Product Specific Information
Positive test controls include: HeLa, HepG2, Jurkat, Mouse lung, Mouse liver, Mouse spleen, Rat lung, Rat liver, Rat kidney. The target is usually found in the following locations: Cytoplasm.
Immunogen sequence: PELQNLLLDD FFKSAVENCQ DSWRRAVSTG VQAGIPMPCF TTALSFYDGY RHEMLPASLI QAQRDYFGAH TYELLAKPGQ FIHTNWTGHG GTVSSSSYNA
Target Information
6-phosphogluconate dehydrogenase is the second dehydrogenase in the pentose phosphate shunt. Deficiency of this enzyme is generally asymptomatic, and the inheritance of this disorder is autosomal dominant. Hemolysis results from combined deficiency of 6-phosphogluconate dehydrogenase and 6-phosphogluconolactonase suggesting a synergism of the two enzymopathies.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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