Phospho-STK39 (Ser311) Antibody
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中文名稱：磷酸化-STK39 (Ser311)兔多克隆抗體
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貨號：CSB-PA029718
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規格：￥2454
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圖片：
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Western blot analysis of extracts from COLO cells using STK39 (Phospho-Ser309) Antibody.The lane on the right is treated with the antigen-specific peptide. -
Immunohistochemical analysis of paraffin-embedded human brain tissue using STK39 (Phospho-Ser309) antibody (left)or the same antibody preincubated with blocking peptide (right).
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其他：
產品詳情
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產品名稱：Rabbit anti-Homo sapiens (Human) STK39 Polyclonal antibody
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Uniprot No.：
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基因名：STK39
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宿主：Rabbit
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反應種屬：Human,Mouse,Rat
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免疫原：Peptide sequence around phosphorylation site of Serine 311(S-F-R(p)-K-L) derived from Human STK39.
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免疫原種屬：Homo sapiens (Human)
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克隆類型：Polyclonal
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純化方式：Antibodies were produced by immunizing rabbits with synthetic phosphopeptide and KLH conjugates. Antibodies were purified by affinity-chromatography using epitope-specific phosphopeptide. Non-phospho specific antibodies were removed by chromatogramphy usi
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濃度：It differs from different batches. Please contact us to confirm it.
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產品提供形式：Liquid
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應用范圍：ELISA,WB,IHC
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推薦稀釋比：
Application Recommended Dilution WB 1:500-1:1000 IHC 1:50-1:100 -
Protocols：
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儲存條件：Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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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.
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用途：For Research Use Only. Not for use in diagnostic or therapeutic procedures.
產品評價
相關產品
靶點詳情
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功能：May act as a mediator of stress-activated signals. Mediates the inhibition of SLC4A4, SLC26A6 as well as CFTR activities by the WNK scaffolds, probably through phosphorylation. Phosphorylates RELT.
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基因功能參考文獻：
- SNP rs1468326 of WNK1, rs6749447 of STK39, and WNK1 haplotype AGACAGGAATCGT were associated with hypertension in Tibetan individuals PMID: 28945285
- STK39 polymorphisms are not associated with Parkinson's disease, ALS and multiple system atrophy in Chinese population. PMID: 29564728
- the polycomb repressor complex is essential for EBNA3A-mediated repression of STK39 Findings in this study provide new insights into the regulation of cellular genes by the transcription factor EBNA3A. PMID: 29367247
- STK39 acts as a tumor oncogene in non-small cell type lung cancer and can be a potential biomarker of carcinogenesis. PMID: 27542260
- In conclusion, these meta-analytical findings suggest that STK39 might not be a hypertension-susceptibility gene. PMID: 27142475
- Here, we report our replication data showing a significant association of the rs3754777 polymorphism, but not rs35929607, of STK39 with essential hypertension in a male Chinese Han population. PMID: 26911228
- did not observe any significant difference in allele and genotype distribution between Parkinson's disease patients and controls for rs1955337 in STK39 PMID: 26914237
- Single nucleotide polymorphisms STK39 and WNK1 were associated with hypertension and BP in our multicenter Belgian case-control study PMID: 27082544
- STK39 mRNA and protein express abnormally in primary hypertension patients with genetic variation, which is related to the blood pressure. PMID: 26662444
- SPAK protein has both the potential to up-regulate KCNQ1/E1 protein abundance in the cell membrane, an effect possibly participating in the regulation of cell volume, excitability, epithelial transport and metabolism. PMID: 26584301
- These observations establish that the CCT domain plays a crucial role in controlling SPAK activity and BP. PMID: 25994507
- Findings indicate that the serine threonine kinase 39 (STK39) mRNA expression is increased in rs3754777 knockin cell lines. PMID: 26416847
- These findings suggested that the STK39 rs1955337 TT genotype is a risk factor for Han-Chinese patients with PD in Taiwan PMID: 26469904
- Taken together, our findings suggest the potential interactive role of STK39 gene multiple polymorphisms in the development of hypertension among northeastern Han Chinese. PMID: 24873805
- In Chinese children, no association of CSK rs1378942, MTHFR rs1801133, CYP17A1 rs1004467, STK39 rs3754777 and FGF5 rs16998073 with BP/risk of hypertension. PMID: 23759979
- SPAK short forms in the kidney are created by aspartyl aminopeptidase (Dnpep)-mediated proteolytic cleavage PMID: 25164821
- the association of the loci rs11711441 near STK39 and sporadic Parkinson disease in the Chinese Han population is confirmed PMID: 24631562
- STK39 (rs2102808) and CCDC62/HIP1R (rs12817488) do not appear to influence PD risk. PMID: 24312176
- SPAK isoforms both inhibit NKCC1 and NKCC2 activity (cation cotransporter)that may be important in renal physiology. PMID: 24133122
- A significant association between STK39 genetic variant rs6749447 and hypertension was found in a Finnish cohort. PMID: 23235358
- Essential hypertension risk conferred by STK39 rs35929607 polymorphism *A/G) was different from that previously reported in a European population. PMID: 23894895
- study found no evidence that STK39 was associated with hypertension in the Chinese population PMID: 23151749
- The present meta-analysis confirms the significant association of STK39 polymorphism with susceptibility to hypertension in Europeans and East Asians. PMID: 23527223
- SPAK and OSR1, which are oftencoexpressed in cells can form functional heterodimers. PMID: 23034389
- STK39 is an independent risk factor for hypertension in men and its intragenic single nucleotide polymorphisms can interact and function in the control of blood pressure. PMID: 20889219
- our results suggest no significant assocation between any of the core autism symptom domains or the four additional previously identified familial features and the rs1807984 SNP on the STK39 gene. PMID: 21442361
- SPAK increases intestinal epithelial permeability; both SPAK-transfected Caco2-cells and SPAK transgenic mice exhibit loss of intestinal barrier function and homeostasis in inflammatory bowel disease. PMID: 21705622
- Serine/threonine kinase 39 is a candidate gene for primary hypertension especially in women. PMID: 21178783
- phosphorylation-induced activation of NKCC1 by osmotic shrinkage does not involve AMP-activated protein kinase and is likely to be due to STE20/SPS1-related proline/alanine-rich kinase activation PMID: 20442269
- STK39 expression is modified by polymorphisms acting in cis and the typed SNPs are associated with allelic expression of this gene, but there is no evidence for an association with blood pressure in a British Caucasian cohort PMID: 20003416
- roles in phosphorylation and activation of the Na-K-Cl cotransporter (NKCC1) PMID: 12740379
- TNF-related apoptosis-inducing ligand down-regulation of SPAK is an important event that enhances its apoptotic effects PMID: 16950202
- evidence for linkage and association between autism and loci within the 2q24-q33 region, including at STK39 PMID: 18348195
- PKCdelta acts upstream of SPAK to increase activity of NKCC1 during hyperosmotic stress PMID: 18550547
- During inflammatory conditions, TNF-alpha is a key regulator of SPAK expression. PMID: 18787102
- variants in STK39 may influence blood pressure by increasing STK39 expression and consequently altering renal Na(+) excretion PMID: 19114657
- data suggest that SPAK, the transcription of which is regulated by hyperosmolarity, plays an important role in epithelial barrier function PMID: 19343169
- Brain WNK3 acts in tandem with SPAK, whereas renal WNK3 seems to upregulate NCCT through a SPAK-independent pathway. PMID: 19470686
- SPAK loss in B-cell lymphomas promotes increased cell survival with DNA damage and provides a potential mechanism for increased resistance to genotoxic stress in cancer. PMID: 19717643
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亞細胞定位：Cytoplasm. Nucleus.
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蛋白家族：Protein kinase superfamily, STE Ser/Thr protein kinase family, STE20 subfamily
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組織特異性：Predominantly expressed in brain and pancreas followed by heart, lung, kidney, skeletal muscle, liver, placenta and testis.
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