Thermo Fisher Scientific ALDH18A1/P5CS Polyclonal Antibody
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
A304803A | - | Thermo Fisher Scientific A304803A ALDH18A1/P5CS Polyclonal Antibody 100 ul pk | 재고문의 | pk | 661,000원 | - | 727,100원 | |
A304803AT | - | Thermo Fisher Scientific A304803AT ALDH18A1/P5CS Polyclonal Antibody 10 ul pk | 재고문의 | pk | 195,000원 | - | 214,500원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
Assay-dependent
Immunoprecipitation (IP)
2-10 µg/mg lysate
Product Specifications
Species Reactivity
Human
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Region between residue 745 to 795 of human Aldehyde Dehydrogenase 18 Family, Member A1. if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
ALDH18A1,
uniProtId:
P54886-1,
ncbiNodeId:
9606,
antigenRange:
745-795,
antigenLength:
795,
antigenImageFileName:
A304-803A_ALDH18A1_P54886-1_Rabbit.svg,
antigenImageFileNamePDP:
A304-803A_ALDH18A1_P54886-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
1 mg/mL
Purification
Antigen affinity chromatography
Storage buffer
phosphate/tris citrate, pH 7-8
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 Orangutan
Target Information
This gene is a member of the aldehyde dehydrogenase family and encodes a bifunctional ATP- and NADPH-dependent mitochondrial enzyme with both gamma-glutamyl kinase and gamma-glutamyl phosphate reductase activities. The encoded protein catalyzes the reduction of glutamate to delta1-pyrroline-5-carboxylate, a critical step in the de novo biosynthesis of proline, ornithine and arginine. Mutations in this gene lead to hyperammonemia, hypoornithinemia, hypocitrullinemia, hypoargininemia and hypoprolinemia and may be associated with neurodegeneration, cataracts and connective tissue diseases. Alternatively spliced transcript variants, encoding different isoforms, have been described for this gene.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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