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 |
PA581862 | - | Thermo Fisher Scientific PA581862 G6PD Polyclonal Antibody 100 ul pk | 재고문의 | pk | 764,000원 | - | 840,400원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
0.04-0.4 µg/mL
Immunohistochemistry (Paraffin) (IHC (P))
1:500-1:1,000
Immunocytochemistry (ICC/IF)
0.25-2 µg/mL
Product Specifications
Species Reactivity
Human
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Recombinant protein corresponding to Human G6PD. Recombinant protein control fragment (Product #RP-91906). if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
G6PD,
uniProtId:
P11413-1,
ncbiNodeId:
9606,
antigenRange:
368-477,
antigenLength:
515,
antigenImageFileName:
PA5-81862_G6PD_P11413-1_Rabbit.svg,
antigenImageFileNamePDP:
PA5-81862_G6PD_P11413-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
0.1 mg/mL
Purification
Antigen affinity chromatography
Storage buffer
PBS, pH 7.2, with 40% glycerol
Contains
0.02% 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_2789023
Product Specific Information
Immunogen sequence: EVRLQFHDVA GDIFHQQCKR NELVIRVQPN EAVYTKMMTK KPGMFFNPEE SELDLTYGNR YKNVKLPDAY ERLILDVFCG SQMHFVRSDE LREAWRIFTP LLHQIELEKP
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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