DISC1 Antibody

中文名稱：

DISC1兔多克隆抗體
貨號：

CSB-PA889093LA01HU
規格：

￥440
圖片：
Western Blot
Positive WB detected in: SH-SY5Y whole cell lysate, Hela whole cell lysate
All lanes: DISC1 antibody at 2μg/ml
Secondary
Goat polyclonal to rabbit IgG at 1/50000 dilution
Predicted band size: 94, 92, 74, 39, 83, 63, 61, 76, 73, 38, 22 kDa
Observed band size: 94, 92, 38 kDa

Immunofluorescent analysis of Hela cells using CSB-PA889093LA01HU at dilution of 1:100 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L)
其他：

產品詳情
產品評價
相關產品
靶點詳情

產品詳情

產品名稱：

Rabbit anti-Homo sapiens (Human) DISC1 Polyclonal antibody
Uniprot No.：

Q9NRI5
基因名：

DISC1
別名：

C1orf136 antibody; DISC1 antibody; DISC1_HUMAN antibody; Disrupted in schizophrenia 1 antibody; Disrupted in schizophrenia 1 protein antibody; KIAA0457 antibody; RP4-730B13.1 antibody; SCZD9 antibody
宿主：

Rabbit
反應種屬：

Human
免疫原：

Recombinant Human Disrupted in schizophrenia 1 protein (99-325AA)
免疫原種屬：

Homo sapiens (Human)

標記方式：

Non-conjugated

本頁面中的產品，DISC1 Antibody (CSB-PA889093LA01HU)，的標記方式是Non-conjugated。對于DISC1 Antibody，我們還提供其他標記。見下表：

標記方式	貨號	產品名稱	應用
HRP	CSB-PA889093LB01HU	DISC1 Antibody, HRP conjugated	ELISA
FITC	CSB-PA889093LC01HU	DISC1 Antibody, FITC conjugated
Biotin	CSB-PA889093LD01HU	DISC1 Antibody, Biotin conjugated	ELISA

克隆類型：

Polyclonal
抗體亞型：

IgG
純化方式：

>95%, Protein G purified
濃度：

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

Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
產品提供形式：

Liquid
應用范圍：

ELISA, WB, IF

推薦稀釋比：

Application	Recommended Dilution
WB	1:2000-1:10000
IF	1:50-1:200

Protocols：

ELISA Protocol
Western Blotting (WB) Protocol
Immunofluorescence (IF) 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.

產品評價

靶點詳情

功能：

Involved in the regulation of multiple aspects of embryonic and adult neurogenesis. Required for neural progenitor proliferation in the ventrical/subventrical zone during embryonic brain development and in the adult dentate gyrus of the hippocampus. Participates in the Wnt-mediated neural progenitor proliferation as a positive regulator by modulating GSK3B activity and CTNNB1 abundance. Plays a role as a modulator of the AKT-mTOR signaling pathway controlling the tempo of the process of newborn neurons integration during adult neurogenesis, including neuron positioning, dendritic development and synapse formation. Inhibits the activation of AKT-mTOR signaling upon interaction with CCDC88A. Regulates the migration of early-born granule cell precursors toward the dentate gyrus during the hippocampal development. Inhibits ATF4 transcription factor activity in neurons by disrupting ATF4 dimerization and DNA-binding. Plays a role, together with PCNT, in the microtubule network formation.
基因功能參考文獻：
1. Significant effect of truncated hDISC1 on glial identity cells along the rostrocaudal axis and their oligodendrocytes specification; appearance of hindbrain oligodendrocyte lineage cells and their premature differentiation may affect cerebrocortical organization and contribute to the pathophysiology of SZ. PMID: 28981898
2. Study shows that DISC1-mutant cerebral organoids display disorganized structural morphology and impaired proliferation, which is phenocopied by WNT agonism and rescued by WNT antagonism. PMID: 29643329
3. Results suggest that DISC1 may be involved in the regulation of lactate production in astrocytes to support neuronal activity and associated behaviors. PMID: 29643356
4. This study showed several gene expression profiles, including DISC1, are associated with age-related changes in White Matter disconnectivity. PMID: 28946750
5. DISC1 overexpression and misassembly is associated with deficits in long-term memory and attention-related behavior in a tgDISC1 rat model. PMID: 29107702
6. Findings showed that NOS1AP (rs348624, rs12742393 and rs1415263), DISC1 (rs821633 and rs1000731), DAOA (rs2391191) and GSK3B (rs6438552) SNPs had no association with development of early-onset schizophrenia; however, our finding suggested statistically significant role of the interaction of NOS1AP, DISC1, DAOA and GSK3B polymorphisms in schizophrenia susceptibility. PMID: 29100974
7. Meta-analysis found that DISC1 polymorphisms increased a risk of schizophrenia, especially in the Chinese population. PMID: 29031911
8. DISC1 a key molecular lead in psychiatry and neurodevelopment. PMID: 27595595
9. The nervous system developmental pathway is a potential pathogenesis of sporadic amyotrophic lateral sclerosis, among them, the polymorphism of rs3737597 in DISC1 might play some roles. PMID: 27052956
10. meta-analysis analyzed the association between DISC1 SNPs rs3738401 and rs821616 with schizophrenia. We found that rs3738401 did not show association with schizophrenia in the Caucasian, Asian or Japanese subgroups PMID: 29410289
11. DISC1 affects glioblastoma cell development via mitochondria dynamics partly by down regulation of Drp1. PMID: 27852062
12. In combination with molecular modeling, data support predictions regarding the three-dimensional fold of a DISC1 segment as well as its steric arrangement in complex with a llama heavy chain antibody. PMID: 29324815
13. Authors found that three pathways that include the homologs of Drosophila Dys, Trio, and Shot were downregulated by introducing a C-terminal truncated mutant DISC1. PMID: 28472294
14. disrupting DISC1/Ndel1 complex formation prolongs mitotic length and interferes with cell-cycle progression in human cells, and it causes cell-cycle deficits of radial glial cells in the embryonic mouse cortex and human forebrain organoids PMID: 29103808
15. Study reports sex-specific influence of common disrupted-in-schizophrenia-1 variants on volumes of the basal ganglia, the amygdala and on the cortical surface area. PMID: 27369464
16. Study found a significant association between the DISC1 gene polymorphism rs6675281 alone, and the combination of rs6675281 and rs821616, and differences in long-term cortical thickness growth in patients with a first-episode of psychosis; and observed an overall difference in cortical thickness, as well as heightened disparities in the frontal and temporal brain regions. PMID: 26209938
17. HTT forms a ternary protein complex with the scaffolding protein DISC1 and cAMP-degrading phosphodiesterase 4 (PDE4) to regulate PDE4 activity. PMID: 28263187
18. This theme highlights the importance of understanding precisely how DISC1 can regulate intracellular trafficking, and suggests that a novel approach to the treatment of psychiatric disorders could be provided by targeting this protein and the trafficking machinery with which it interacts. PMID: 27121900
19. Findings indicate that disrupted-in-schizophrenia 1 (DISC1) and close homolog of L1 may engage in physical and functional interaction in neural development, supporting the notion that DISC1 regulates neurite outgrowth with a receptor belonging to the neural cell adhesion molecules. PMID: 27346367
20. DISC1 increased the risk for late-onset Alzheimer's disease in northern Han Chinese population. PMID: 27023224
21. Findings suggest that synapse-associated protein of 97-kDa molecular weight and disrupted in schizophrenia 1 contribute to maintaining Wnt/beta-catenin signaling activity within a homeostatic range by regulating glycogen synthase kinase 3 beta phosphorylation. PMID: 27026592
22. DISC1 has distinctly folded regions, which are bisected by mental illness-related mutations PMID: 28249940
23. These results should contribute to reveal DISC1 physiological function and potential pathogenic role in severe mental illnesses PMID: 27466199
24. This population-based case-control study was carried out to determine whether polymorphisms in DISC1 and NRG1 genes could be associated with schizophrenia in the Chinese population. PMID: 27236031
25. This study demonstrated that the Increased density of DISC1-immunoreactive oligodendroglial cells in fronto-parietal white matter of patients with paranoid schizophrenia. PMID: 26315603
26. The present findings, at least in part, provide some clues for further investigating the association of DISC1 variants with SCZ susceptibility PMID: 26945459
27. DISC1 may be involved in sleep regulation PMID: 27354230
28. Polymorphisms in DISC1 play a role in vulnerability to opioid dependence in a Polish sample. PMID: 26997180
29. Hypoxic preconditioning decreases NF-kappaB activity via DISC1. PMID: 26615762
30. It is anterogradely transported to the neurite tips, together with Lis1, and functions in neurite extension via suppression of GSK3beta activity. PMID: 27333658
31. DISC1 disruption affects expression of neural cell fate markers and Wnt signaling. PMID: 26299970
32. These results uncover an unexpected role for DISC1 in normal beta-cell physiology and suggest that DISC1 dysregulation contributes to T2D independently of its importance for cognition. PMID: 26546129
33. DISC1 gene variations may affect the course of cognitive deficits found in patients suffering from the first episode of non-affective psychosis PMID: 26443054
34. DISC1 acts as an important regulator of mitochondrial dynamics in both axons and dendrites. PMID: 26553875
35. An association was found with DISC1 genetic variants and susceptibility to schizophrenia in a Han Chinese population. PMID: 26162659
36. Results with immature neurons from patients with schizophrenia and bipolar disorder showed common alterations in DISC1 levels and its cellular distribution, cAMP homeostasis, and cell migration PMID: 25620115
37. results demonstrate that DISC1 protein levels in human lymphocytes are correlated with the diagnosis of schizophrenia independent of smoking and thus present a potential biomarker PMID: 25218871
38. The results of this student findings provide consistent evidence that the DISC1 Ser704Cys polymorphism influences the thalamic-prefrontal circuits in humans. PMID: 24146131
39. Transient neonatal disruption of signaling via the C-terminal domain of "disrupted in schizophrenia 1" (DISC1)-a molecule implicated in psychiatric disorders-resulted in a lack of long-term potentiation (LTP) (persistent strengthening of synapses) and experience-dependent potentiation in adulthood. PMID: 26206934
40. We demonstrated that Ser704Cys-genotype of DISC1 influences (para)hippocampal structure and functioning the dorsal PFC during executive planning, most prominently in unaffected controls PMID: 25533973
41. Our results revealed association between rare haplotypes and affective disorder providing further support to the hypothesis that DISC1 sequence variations may be related to AD susceptibility PMID: 24090488
42. These results suggested a possible role of the DISC1 genotype in the early neurodevelopment of human brains, but failed to show its specific role in the neurodevelopmental pathology of schizophrenia. PMID: 25092219
43. In Disc1-knockout mice, recombinant human DISC1 regulates the dendritic transport of Itpr1 mRNA by directly interacting with its mRNA. PMID: 25821909
44. In the adult mammalian brain DISC1 plays a critical role in neurite outgrowth and neuronal migration, particularly in the hippocampus. PMID: 25043320
45. DISC1 knockdown leads to a reduction of VGF in neurons. PMID: 24934694
46. These findings highlight the importance of the coordinated expression of DISC1-interactome genes for normal cognitive function. PMID: 24940743
47. This study provided that DISC1 genetic variants reveals a relationship with the structure and functional connectivity of the precuneus in schizophrenia. PMID: 24909300
48. Expression of the DB7 fusion gene may reduce protein translation to impair brain functions and thereby contribute to the pathogenesis of major psychiatric disorders. PMID: 24908665
49. DISC1 forms a complex with dysbindin and increases its stability in association with a reduction in ubiquitylation. PMID: 25635053
50. The results reinforce the role of DISC1 in the association of schizophrenia PMID: 23855403
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相關疾病：

Schizophrenia 9 (SCZD9)
亞細胞定位：

Cytoplasm. Cytoplasm, cytoskeleton. Mitochondrion. Cytoplasm, cytoskeleton, microtubule organizing center, centrosome. Cell junction, synapse, postsynaptic density.
組織特異性：

Ubiquitous. Highly expressed in the dentate gyrus of the hippocampus. Also expressed in the temporal and parahippocampal cortices and cells of the white matter.
數據庫鏈接：

HGNC: 2888

OMIM: 604906

KEGG: hsa:27185

STRING: 9606.ENSP00000355593

UniGene: Hs.13318

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