DNAAF4 Antibody

中文名稱：

DNAAF4兔多克隆抗體
貨號：

CSB-PA855504LA01HU
規格：

￥440
圖片：
Western Blot
Positive WB detected in: HepG2 whole cell lysate, Hela whole cell lysate, Mouse brain tissue
All lanes: DNAAF4 antibody at 3.4µg/ml
Secondary
Goat polyclonal to rabbit IgG at 1/50000 dilution
Predicted band size: 49, 45 kDa
Observed band size: 49 kDa

Immunohistochemistry of paraffin-embedded human testis tissue using CSB-PA855504LA01HU at dilution of 1:100

Immunofluorescent analysis of Hela cells using CSB-PA855504LA01HU 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) DNAAF4 Polyclonal antibody
Uniprot No.：

Q8WXU2
基因名：

DNAAF4
別名：

Dyslexia susceptibility 1 candidate 1 antibody; Dyslexia susceptibility 1 candidate gene 1 protein antibody; DYX1 antibody; DYX1C1 antibody; DYXC1 antibody; DYXC1_HUMAN antibody; EKN1 antibody; FLJ37882 antibody; MGC70618 antibody; RD antibody
宿主：

Rabbit
反應種屬：

Human, Mouse
免疫原：

Recombinant Human Dynein assembly factor 4, axonemal protein (109-295AA)
免疫原種屬：

Homo sapiens (Human)

標記方式：

Non-conjugated

本頁面中的產品，DNAAF4 Antibody (CSB-PA855504LA01HU)，的標記方式是Non-conjugated。對于DNAAF4 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-PA855504LB01HU	DNAAF4 Antibody, HRP conjugated	ELISA
FITC	CSB-PA855504LC01HU	DNAAF4 Antibody, FITC conjugated
Biotin	CSB-PA855504LD01HU	DNAAF4 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, IHC, IF

推薦稀釋比：

Application	Recommended Dilution
WB	1:500-1:5000
IHC	1:20-1:200
IF	1:50-1:200

Protocols：

ELISA Protocol
Western Blotting (WB) Protocol
Immunohistochemistry (IHC) 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：

Axonemal dynein assembly factor required for ciliary motility. Involved in neuronal migration during development of the cerebral neocortex. May regulate the stability and proteasomal degradation of the estrogen receptors that play an important role in neuronal differentiation, survival and plasticity.
基因功能參考文獻：
1. that endogenous DYX1C1 localizes to the base of the cilium, whereas DCDC2 localizes along the entire axoneme of the cilium PMID: 27451412
2. promoter SNP rs12899331 of DYX1C1 may contribute towards the manifestation of DD. This study supports the association of DYX1C1 with DD in an Indian population PMID: 24362368
3. results demonstrate that DYX1C1 can modulate the expression of genes involved in cell migration and nervous system development and associates with a number of cytoskeletal proteins. PMID: 23036959
4. DYX1C1 is required for axonemal dynein assembly and ciliary motility. PMID: 23872636
5. The results of this study do not provide evidence for association between the putatively functional single nucleotide polymorphisms -3G/A and 1249G/T in DYX1C1 and reading disabilities. PMID: 23341075
6. Gene-by-environment effects were found between some specified environmental moderators (i.e. maternal smoke during pregnancy, birth weight and socio-economic status) and the DYX1C1-1259C/G marker PMID: 23176554
7. results suggested that the 931C > T variant in KIAA0319, but not the -3G > A in DYX1C1, was significantly associated with the risk of dyslexia PMID: 23065966
8. DYX1C1 influences reading development in the general Chinese population and supports a universal effect of this gene. PMID: 23028439
9. The results of this study found that DYX1C1 gene contained polymorphisms that were significantly associated with white matter volume in the left temporo-parietal region and that white matter volume influenced reading ability. PMID: 22683091
10. Mutations in cilia co-expressed DCDC2, DYX1C1 and KIAA0319 genes are associated with a cognitive neurological disorder, dyslexia. PMID: 22558177
11. the expression of DYX1C1 in breast cancer is associated with several clinicopathological parameters and that loss of DYX1C1 correlates with a more aggressive disease, in turn indicating that DYX1C1 is a potential prognostic biomarker in breast cancer. PMID: 22375924
12. A single nucleotide polymorphism previously shown to be associated with dyslexia and located in the cis-regulatory region of DYX1C1 may alter the epigenetic and endocrine regulation of this gene. PMID: 22383464
13. findings suggest that DYX1C1 is associated with dyslexia in people of Chinese ethnicity. PMID: 21599957
14. No statistically significant associations were found between DCDC2 or DYX1C1 and language phenotypes. Both DCDC2 and DYX1C1 DD susceptibility genes appear to have a pleiotropic role on mathematics but not language phenotypes. PMID: 21046216
15. At this point, there is no statistical evidence of association between the allelic variation in the three candidate genes and DD in our sample. PMID: 21203818
16. Association signals were detected for several single nucleotide polymorphisms within DYX1C1 with both the reading and spelling tests PMID: 20846247
17. Results suggest that DYX1C1 influences reading and spelling ability with additional effects on short-term information storage or rehearsal. Missense mutation rs17819126 is a potential functional basis for the association of DYX1C1 with dyslexia. PMID: 19901951
18. Functional characterization of the homologous rat protein. PMID: 16989952
19. DYX1C1 should be regarded as a candidate gene for developmental dyslexia and localizes to a fraction of cortical neurons and white matter glial cells PMID: 12954984
20. Findings provide support for EKN1 as a risk locus for dyslexia and as contributing to reading component processes and reading-related abilities. PMID: 15249932
21. Thus it seems unlikely that DYX1C1 gene would be involved in the genetic etiology of autism in Finnish patients. PMID: 15470369
22. DYX1C1 is unlikely to be a susceptibility gene for developmental dyslexia PMID: 15477871
23. Single nucleotide polymorphisms of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs. PMID: 15520411
24. disequilibrium with DYX1C1 is more saliently explained in Italian dyslexics by short-term memory PMID: 17309662
25. The observation of weak evidence for transmission disequilibrium for one of the two studied polymorphisms in DYX1C1 suggests involvement of this gene in dyslexia. PMID: 17450541
26. TFII-I, PARP1, and SFPQ proteins, each previously implicated in gene regulation, form a complex controlling transcription of DYX1C1. Allelic differences in the promoter or 5'UTR of DYX1C1 may affect factor binding and thus regulation of the gene. PMID: 18445785
27. Alternatively spliced transcript variants of the DYX1C1 gene may be used as cancer biomarkers to detect colorectal cancer. PMID: 18618141
28. The contribution of DYX1C1 to dyslexia in a sample of 366 trios of German descent, was investigated. PMID: 19240663
29. The DYX1C1 is a novel Hsp70 and Hsp90-interacting co-chaperone protein and its expression is associated with malignancy. PMID: 19277710
30. DYX1C1 interacts with both ERs in the presence of 17beta-estradiol in neurons. PMID: 19423554
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相關疾病：

Dyslexia 1 (DYX1); Ciliary dyskinesia, primary, 25 (CILD25)
亞細胞定位：

Nucleus. Cytoplasm. Dynein axonemal particle. Cell projection, neuron projection.
組織特異性：

Expressed in several tissues, including brain, lung, kidney and testis. In brain localizes to a fraction of cortical neurons and white matter glial cells.
數據庫鏈接：

HGNC: 21493

OMIM: 127700

KEGG: hsa:161582

STRING: 9606.ENSP00000323275

UniGene: Hs.126403

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