WDR62 Antibody

中文名稱：

WDR62兔多克隆抗體
貨號：

CSB-PA026050LA01HU
規格：

￥440
圖片：
Immunohistochemistry of paraffin-embedded human bladder cancer using CSB-PA026050LA01HU at dilution of 1:100
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) WDR62 Polyclonal antibody
Uniprot No.：

O43379
基因名：

WDR62
別名：

WDR62 antibody; C19orf14 antibody; WD repeat-containing protein 62 antibody
宿主：

Rabbit
反應種屬：

Human
免疫原：

Recombinant Human WD repeat-containing protein 62 protein (889-1188AA)
免疫原種屬：

Homo sapiens (Human)

標記方式：

Non-conjugated

本頁面中的產品，WDR62 Antibody (CSB-PA026050LA01HU)，的標記方式是Non-conjugated。對于WDR62 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-PA026050LB01HU	WDR62 Antibody, HRP conjugated	ELISA
FITC	CSB-PA026050LC01HU	WDR62 Antibody, FITC conjugated
Biotin	CSB-PA026050LD01HU	WDR62 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, IHC

推薦稀釋比：

Application	Recommended Dilution
IHC	1:20-1:200

Protocols：

ELISA Protocol
Immunohistochemistry (IHC) 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：

Required for cerebral cortical development. Plays a role in neuronal proliferation and migration. Plays a role in mother-centriole-dependent centriole duplication; the function seems also to involve CEP152, CDK5RAP2 and CEP63 through a stepwise assembled complex at the centrosome that recruits CDK2 required for centriole duplication.
基因功能參考文獻：
1. Our findings demonstrate critical and diverse functions of WDR62 in neocortical development and provide insight into the mechanisms by which its disruption leads to a plethora of structural abnormalities. PMID: 28272472
2. We report a clinical feature, electroclinical findings, and clinical course of a patient with a severe phenotype of MCPH2 including microcephaly, refractory infantile spasms and intellectual disability. We detected a new homozygous splicing variant c.3335+1G>C in the WD repeat domain 62 (WDR62) gene, and an additional new heterozygous missense mutation c.1706T>A of G protein-coupled receptor 56 (GPR56) gene PMID: 28756000
3. Authors demonstrated that WDR62 is a PLK1 substrate that is phosphorylated at Ser 897, and that this phosphorylation at the spindle poles promotes astral microtubule assembly to stabilize spindle orientation. PMID: 28973348
4. Case Report: WDR62 missence mutations associated with early onset acanthosis and hyperkeratosis in a patient with autosomal recessive microcephaly type 2. PMID: 27852057
5. WDR62-overexpressing lung cancer cells exhibited an increase in cell growth. Moreover, the concurrent overexpression of WDR62 and TPX2, a WDR62-interacting protein that is also overexpressed in lung adenocarcinoma, induced centrosome amplification in the lung cells. PMID: 28277612
6. A novel WDR62 missense mutation causes primary microcephaly in a large consanguineous Saudi family PMID: 28377545
7. The results confirm that mutations in ASPM or WDR62 are the major cause of autosomal recessive primary microcephaly in the Pakistani population. PMID: 27784895
8. Data show that CUL4B variants are associated with a wide range of cerebral malformations and suggest an important role in brain through its interaction with WDR62, a protein in which variants were identified in patients with cerebral malformations. PMID: 25385192
9. Genetic factors contribute to modify the severity of the WDR62 phenotype. PMID: 24842779
10. WDR62 controls neurogenesis through JNK signaling in rat model. PMID: 24388750
11. Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation PMID: 24228726
12. WDR62 may be a novel prognostic marker and a potential chemotherapy target for gastric cancer. PMID: 23920402
13. A homozygous deletion mutation c.1143delA was detected in exon 9 of WDR62 gene, in all affected individuals with primary microcephaly in a Pakistani family, which resulted in frameshift and protein truncation (p.H381PfsX48). PMID: 23065275
14. Data indicate that WDR62 dimerization is required for JNK2 and MKK7beta1 recruitment. PMID: 23341463
15. homozygous missense mutation in WDR62, p.E400K, was found in both boys and segregated with the condition in this family. WDR62 is one of seven genes responsible for autosomal recessive primary microcephaly PMID: 22308068
16. Mutations in WDR62 gene leads to microcephaly and other brain malformations. PMID: 21496009
17. study reports using whole-exome sequencing to identify compound heterozygous mutations in the WD repeat domain 62 (WDR62) gene as the cause of recurrent polymicrogyria in a sibling pair PMID: 21834044
18. data indicate that WDR62 mutations cause about 4% of autosomal recessive primary microcephaly in Pakistan. PMID: 21961505
19. The docking domain of WDR62 interacts with all JNK isoforms through a D domain motif located at the C-terminus. PMID: 21749326
20. Homozygous mutations in WDR62 cause autosomal recessive primary microcephaly in families linked to the MCPH2 locus. This gene encodes a centrosomal as well as nuclear protein. PMID: 21496009
21. The diverse phenotypes of WDR62 suggest it has central roles in many aspects of cerebral cortical development and that mutations cause microencephaly. PMID: 20890278
22. Identification of WDR62 as the second most common cause of second most common cause of autosoml reccessive microcephaly. PMID: 20890279
23. WDR62 mutations found in individuals with microcephaly associated with a broad range of malformations of cortical development. PMID: 20980985
24. Study demonstrates the use of whole-exome sequencing to identify recessive mutations in WD repeat domain 62 (WDR62) as the cause of a wide spectrum of severe cerebral cortical malformations including microcephaly. PMID: 20729831
25. JNK and WDR62 may regulate the dynamic interplay between polysomes stress granule and processing bodies, thereby mediating mRNA fate after stress. PMID: 19910486
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相關疾病：

Microcephaly 2, primary, autosomal recessive, with or without cortical malformations (MCPH2)
亞細胞定位：

Nucleus. Cytoplasm, cytoskeleton, spindle pole. Cytoplasm, cytoskeleton, microtubule organizing center, centrosome. Cytoplasm, cytoskeleton, microtubule organizing center, centrosome, centriole.
組織特異性：

Present in fetal brain, enriched within the ventricular and subventricular zone (at protein level). In the embryonic brain it is expressed in mitotic neural precursor cells.
數據庫鏈接：

HGNC: 24502

OMIM: 604317

KEGG: hsa:284403

STRING: 9606.ENSP00000384792

UniGene: Hs.116244

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