ALDH5A1 Antibody

說明書

中文名稱：

ALDH5A1兔多克隆抗體
貨號：

CSB-PA001577GA01HU
規(guī)格：

￥3,900
其他：

產(chǎn)品詳情
產(chǎn)品評價
相關(guān)產(chǎn)品
靶點詳情

產(chǎn)品詳情

Uniprot No.：

P51649
基因名：

ALDH5A1
別名：

Aldedehyde dehydrogenase 5 family antibody; Aldehyde dehydrogenase 5 family member A1 antibody; Aldehyde dehydrogenase 5A1 antibody; Aldehyde dehydrogenase family 5 member A1 antibody; ALDH5A 1 antibody; Aldh5a1 antibody; mitochondrial antibody; Mitochondrial succinate semialdehyde dehydrogenase antibody; NAD(+) dependent succinic semialdehyde dehydrogenase antibody; NAD(+)-dependent succinic semialdehyde dehydrogenase antibody; SSADH antibody; SSDH antibody; SSDH_HUMAN antibody; Succinate semialdehyde dehydrogenase antibody; Succinate-semialdehyde dehydrogenase antibody
宿主：

Rabbit
反應種屬：

Human,Mouse,Rat
免疫原：

Human ALDH5A1
免疫原種屬：

Homo sapiens (Human)
抗體亞型：

IgG
純化方式：

Antigen Affinity purified
濃度：

It differs from different batches. Please contact us to confirm it.
保存緩沖液：

PBS with 0.1% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
產(chǎn)品提供形式：

Liquid
應用范圍：

ELISA,WB
Protocols：

ELISA Protocol
Western Blotting (WB) Protocol
儲存條件：

Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
貨期：

Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
用途：

For Research Use Only. Not for use in diagnostic or therapeutic procedures.

產(chǎn)品評價

靶點詳情

功能：

Catalyzes one step in the degradation of the inhibitory neurotransmitter gamma-aminobutyric acid (GABA).
基因功能參考文獻：
1. By ALDH5A1 gene expression in transiently transfected HEK293 cells and enzyme activity assays, we demonstrate that the p.V500 L mutation, despite being conservative, produces complete loss of enzyme activity PMID: 28664505
2. ALDH5A1 mRNA expression was down-regulated in ovarian cancer patients compared with that in normal tissues. PMID: 28346042
3. SSADH catalytic loop role in the SSADH redox-switch modulation PMID: 26422261
4. The proband was found to have compound heterozygous mutations of the succinate-semialdehyde dehydrogenase (ALDH5A1) gene, namely c.398_399delAA (p.N134X) and c.638G>T (p.R213L), for which her parents were both heterozygous carriers. PMID: 28186584
5. Two novel ALDH5A1 mutations likely responsible for SSADH deficiency were identified, and DNA sequencing provided an accurate diagnosis for an at-risk fetus whose sibling had SSADH deficiency. Current study and literature review identified nine additional novel mutations in eight unrelated families bringing the number of unique mutations of ALDH5A1 resulting in SSADH deficiency to 44, occurring from exon 1 to exon 10. PMID: 25431891
6. Pearl et al. identify 3 new pathogenic mutations in the ALDH5A1 gene previously unreported in the literature. EXON: 1 Nucleotide change: c.412 C>T Change in protein: p.L138F EXON: 4 Nucleotide change: c.754G>T Change in protein: p.Q252X EXON: 8 Nucleotide change: c.1360G>A Change in protein: p.A454T PMID: 25558043
7. Missense mutation in ALDH5A1 is associated with succinic semialdehyde dehydrogenase deficiency and severe intellectual disability. PMID: 23825041
8. Results show that opioid-dependent patients carrying the T allele of a functional variant in ALDH5A1 had a greater risk of being nonresponders to methadone maintenance treatment PMID: 24230997
9. The strongest association signal arose from an intronic region of the gene ALDH5A1, which encodes the mitochondrial enzyme succinic semialdehyde dehydrogenase (SSADH), an enzyme involved in gamma-aminobutyric acid metabolism. PMID: 24327614
10. Missense mutations of c.527G>A and c.691G>A in the ALDH5A1 gene are associated with pathogenesis of succinic semialdehyde dehydrogenase deficiency. PMID: 23926001
11. Succinic semialdehyde dehydrognase deficiency is caused by a mutation of the Aldh5a1-gene resulting in a dysfunction of the enzyme succinic semialdehyde dehydrogenase--{REVIEW} PMID: 23516105
12. our study identified a novel homozygous ALDH5A1 gene mutation associated with SSADH deficiency. PMID: 22437753
13. Study seeks to determine whether cerebellar abnormalities are present in human succinic semialdehyde dehydrogenase deficiency on volumetric MRI, compared with radiographic and histologic studies in the mouse model. PMID: 20445195
14. the duplication (6)(p22.2) and corresponding hyperactive level of SSADH activity may have negative consequences for GABA metabolism PMID: 21438145
15. This study indicated that global disruption of cortical networks in SSADH KO mice, affecting both excitatory and inhibitory neurons. PMID: 20363598
16. High activity of this protein probably indicates disorders in lymphocyte energy state. PMID: 12629812
17. Higher SSADH activity is associated with higher intelligence across the general population. PMID: 14981524
18. The unexpected pattern of human SSADH polymorphism compared to interspecific findings outlines the possibility of a recent positive selection on some variants relevant to new cognitive capabilities unique to humans. PMID: 16786440
19. Deficiency in humans causes ggamma-hydroxybutyric aciduria. PMID: 17457693
20. within the 65-85 years age range, the T/T genotype is overrepresented in subjects with impaired cognitive function PMID: 18505418
21. Redox-switch modulation of human SSADH by dynamic catalytic loop PMID: 19300440
22. SSADH deficient patients have widespread reduction in benzodiazepine receptor (BZPR) binding, suggested by high endogenous brain GABA levels that downregulate GABA(A)-BZPR binding site availability. PMID: 19667317
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相關(guān)疾病：

Succinic semialdehyde dehydrogenase deficiency (SSADHD)
亞細胞定位：

Mitochondrion.
蛋白家族：

Aldehyde dehydrogenase family
組織特異性：

Brain, pancreas, heart, liver, skeletal muscle and kidney. Lower in placenta.
數(shù)據(jù)庫鏈接：

HGNC: 408

OMIM: 271980

KEGG: hsa:7915

STRING: 9606.ENSP00000314649

UniGene: Hs.371723

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