Thermo Fisher Scientific AMPD3 Polyclonal Antibody
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
PA565218 | - | Thermo Fisher Scientific PA565218 AMPD3 Polyclonal Antibody 100 ul pk | 재고문의 | pk | 794,000원 | - | 873,400원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Immunocytochemistry (ICC/IF)
0.25-2 µg/mL
Product Specifications
Species Reactivity
Human
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Recombinant Human AMPD3. Recombinant protein control fragment (Product #RP-104691). if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
AMPD3,
uniProtId:
Q01432-1,
ncbiNodeId:
9606,
antigenRange:
208-283,
antigenLength:
767,
antigenImageFileName:
PA5-65218_AMPD3_Q01432-1_Rabbit.svg,
antigenImageFileNamePDP:
PA5-65218_AMPD3_Q01432-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
0.05 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_2663127
Product Specific Information
Immunogen sequence: PYCLDDAPPNL DYLVHMQGGI LFVYDNKKML EHQEPHSLPY PDLETYTVDM SHILALITDG PTKTYCHRRL NFLES
Highest antigen sequence identity to the following orthologs - mouse 89%, rat 89%.
Target Information
AMPD3 is a member of the AMP deaminase gene family. This protein is a highly regulated enzyme that catalyzes the hydrolytic deamination of adenosine monophosphate to inosine monophosphate, a branch point in the adenylate catabolic pathway. The protein is the erythrocyte (E) isoforms, whereas other family members isoforms predominate in muscle (M) and liver (L) cells. Mutations in this gene lead to the clinically asymptomatic, autosomal recessive condition erythrocyte AMP deaminase deficiency.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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