Thermo Fisher Scientific ALDH3A2 Monoclonal Antibody (OTI2A7), TrueMAB
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
TA503256 | - | Thermo Fisher Scientific TA503256 ALDH3A2 Monoclonal Antibody (OTI2A7), TrueMAB 100 ul pk | 재고문의 | pk | 628,000원 | - | 690,800원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
1:500
Immunohistochemistry (Paraffin) (IHC (P))
1:150
Flow Cytometry (Flow)
1:100
Product Specifications
Species Reactivity
Human
Host/Isotype
Mouse / IgG2b
Class
Monoclonal
Type
Antibody
Clone
OTI2A7
Immunogen
Full length human recombinant protein of human ALDH3A2 produced in HEK293T cell. if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
ALDH3A2,
uniProtId:
P51648-1,
ncbiNodeId:
9606,
antigenRange:
1-485,
antigenLength:
485,
antigenImageFileName:
TA503256_ALDH3A2_P51648-1_House_mouse.svg,
antigenImageFileNamePDP:
TA503256_ALDH3A2_P51648-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
0.62 mg/mL
Purification
Affinity chromatography
Storage buffer
PBS with 1% BSA, 50% glycerol
Contains
0.02% sodium azide
Storage conditions
-20° C, Avoid Freeze/Thaw Cycles
Shipping conditions
Ambient (domestic); Wet ice (international)
Target Information
Aldh3A2 is a member of the aldehyde dehydrogenase superfamily, a group of NAD(P)(+)-dependent enzymes that catalyze the oxidation of a wide spectrum of aliphatic and aromatic aldehydes. Aldehyde dehydrogenase enzymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. Aldh3A2 catalyzes the oxidation of long-chain aliphatic aldehydes to fatty acids. Mutations in the Aldh3A2 gene cause Sjogren-Larrson syndrome, an inherited neurocutaneous disorder. Patients with this disorder display ichthyosis, mental retardation and spastic diplegia. The pathogenesis of the cutaneous and neurological symptoms is thought to result from abnormal lipid accumulation in the membranes of skin and brain, the formation of aldehyde Schiff base adducts with amine-containing lipids or proteins, or defective eicosanoid metabolism.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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