NEK1 Antibody

說明書

中文名稱：

NEK1兔多克隆抗體
貨號：

CSB-PA444209
規格：

￥1100
圖片：
The image on the left is immunohistochemistry of paraffin-embedded Human lymphoma tissue using CSB-PA444209(NEK1 Antibody) at dilution 1/25, on the right is treated with synthetic peptide. (Original magnification: ×200)

The image on the left is immunohistochemistry of paraffin-embedded Human lung cancer tissue using CSB-PA444209(NEK1 Antibody) at dilution 1/25, on the right is treated with synthetic peptide. (Original magnification: ×200)
其他：

產品詳情
產品評價
相關產品
靶點詳情

產品詳情

Uniprot No.：

Q96PY6
基因名：

NEK1
別名：

DKFZp686D06121 antibody; DKFZp686K12169 antibody; kat antibody; KIAA1901 antibody; MGC138800 antibody; MGC189817 antibody; NEK1 antibody; NEK1_HUMAN antibody; Never in mitosis A-related kinase 1 antibody; Never in mitosis gene A-related kinase 1 antibody; NIMA (never in mitosis gene a)-related kinase 1 antibody; NIMA-related kinase 1 antibody; NimA-related protein kinase 1 antibody; NY-REN-55 antibody; OTTHUMP00000219432 antibody; OTTHUMP00000219433 antibody; OTTHUMP00000219434 antibody; OTTHUMP00000219435 antibody; Protein-serine/threonine kinase antibody; Renal carcinoma antigen NY-REN-55 antibody; Serine/threonine-protein kinase Nek1 antibody; SRPS2 antibody; SRPS2A antibody; SRTD6 antibody
宿主：

Rabbit
反應種屬：

Human,Mouse
免疫原：

Synthetic peptide of Human NEK1
免疫原種屬：

Homo sapiens (Human)
標記方式：

Non-conjugated
抗體亞型：

IgG
純化方式：

Antigen affinity purification
濃度：

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

-20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol
產品提供形式：

Liquid
應用范圍：

ELISA,IHC

推薦稀釋比：

Application	Recommended Dilution
ELISA	1:2000-1:5000
IHC	1:25-1:100

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：

Phosphorylates serines and threonines, but also appears to possess tyrosine kinase activity. Involved in DNA damage checkpoint control and for proper DNA damage repair. In response to injury that includes DNA damage, NEK1 phosphorylates VDAC1 to limit mitochondrial cell death. May be implicated in the control of meiosis. Involved in cilium assembly.
基因功能參考文獻：
1. We provide novel evidence for association of NEK1 with ALS in Chinese, reporting variants in these genes not previously found in Europeans. PMID: 29149916
2. NEK1 variants may modify disease presentation of driving mutations. PMID: 28935222
3. Following DNA damage, addition of the TLK1 inhibitor, THD, or overexpression of NEK1-T141A mutant impaired ATR and Chk1 activation, indicating the existence of a TLK1>NEK1>ATR>Chk1 pathway. Indeed, overexpression of the NEK1-T141A mutant resulted in an altered cell cycle response after exposure of cells to oxidative stress, including bypass of G1 arrest and implementation of an intra S-phase checkpoint. PMID: 28426283
4. This study shown that the NEK1 is a novel in patient with familial amyotrophic lateral sclerosis. PMID: 26945885
5. Mutation in NEK1 gene is associated with amyotrophic lateral sclerosis. PMID: 27455347
6. Nek1 phosphorylates Rad54 and regulates Rad51 removal to orchestrate homologous recombination and replication fork stability. PMID: 27264870
7. Compound heterozygous variants in NEK1 were identified in two brothers with Mohr syndrome. The nonsense variant c.1226G>A, p.(Trp409*), results in nonsense-associated alternative splicing. Ciliation in patient fibroblasts is drastically reduced. PMID: 27530628
8. The skeletal phenotype of our patient was milder than those of previously reported cases with NEK1 mutations and those with axial SMD harboring C21orf2 mutations. Phenotypes associated with NEK1 mutations are variable and the phenotype-genotype corelation in skeletal ciliopathies is challenging PMID: 28123176
9. Nek1 overexpression in gliomas was correlated with the proliferation marker (Ki-67), tumor grade, Karnofsky performance scale (KPS) and more importantly, patients' poor survival. Further studies showed that Nek1 expression level was also increased in multiple glioma cell lines (U251-MG, U87-MG, U118, H4 and U373). PMID: 27251576
10. C21ORF2 functions in the same pathway as NEK1 in DNA damage repair. PMID: 26290490
11. Nek1 may facilitate S-phase progression by interacting with Ku80 and regulating chromatin loading of replication factors. PMID: 23851348
12. Nek1 may suppress cilia by phosphorylating pVHL, which is critical to microtubule stabilization and ciliary stability. PMID: 23255108
13. as an ATR-associated kinase, Nek1 enhances the stability and activity of ATR-ATRIP before DNA damage, priming ATR-ATRIP for a robust DNA damage response PMID: 23345434
14. The present case provides evidence for a correlation of NEK1 mutation with short rib-polydactyly syndrome type II (Majewski. PMID: 22482978
15. This study confirms that NEK1 is one gene causing SRP type II but also reports mutations in DYNC2H1, expanding the phenotypic spectrum of DYNC2H1 mutations. PMID: 22499340
16. results demonstrate that Nek1 is important for proper checkpoint control and characterize for the first time a DNA damage response that does not directly involve one of the known upstream mediator kinases, ATM or ATR PMID: 21301226
17. absence of functional full-length NEK1 severely reduces cilia number and alters ciliar morphology in vivo. PMID: 21211617
18. Nek1 is involved in the beginning of the cellular response to genotoxic stress and plays an important role in preventing cell death induced by DNA damage. PMID: 20501547
19. Data report that NEK1 and CLASP2 colocalize with FEZ1 in a perinuclear region in mammalian cells, and observed that coiled-coil interactions occur between FEZ1/CLASP2 and FEZ1/NEK1 in vitro. PMID: 19924516
20. these data provide a mechanism to explain how Nek1 regulates cell death by affecting the opening and closing of VDAC1. PMID: 20230784
21. Mapping studies of NEK1 regulatory domain indicate interaction with most of the proteins known to take part in etiology of polycystic kidney disease, in double-strand DNA break repair at the G2/M cell-cycle transition phase, or in neural cell development. PMID: 14690447
22. Nek1 may function as a kinase early in the DNA damage response pathway. PMID: 15604234
23. These data show that Nek1 is important for efficient DNA damage checkpoint control and for proper DNA damage repair. PMID: 18843199
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相關疾病：

Short-rib thoracic dysplasia 6 with or without polydactyly (SRTD6)
亞細胞定位：

Nucleus. Cytoplasm, cytoskeleton, microtubule organizing center, centrosome. Cytoplasm.
蛋白家族：

Protein kinase superfamily, NEK Ser/Thr protein kinase family, NIMA subfamily
組織特異性：

High fetal expression in the brain and kidney.
數據庫鏈接：

HGNC: 7744

OMIM: 263520

KEGG: hsa:4750

STRING: 9606.ENSP00000424757

UniGene: Hs.481181

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