KCNIP1 Antibody
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货号:CSB-PA585744
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规格:¥880
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图片:
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其他:
产品详情
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Uniprot No.:Q9NZI2
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基因名:KCNIP1
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别名:A type potassium channel modulatory protein 1 antibody; A-type potassium channel modulatory protein 1 antibody; KChIP1 antibody; KCIP1_HUMAN antibody; Kcnip1 antibody; Kv channel interacting protein 1 antibody; Kv channel-interacting protein 1 antibody; MGC9 antibody; MGC95 antibody; Potassium channel interacting protein 1 antibody; Potassium channel-interacting protein 1 antibody; VABP antibody; Vesicle APC binding protein antibody; Vesicle APC-binding protein antibody
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宿主:Rabbit
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反应种属:Human,Mouse
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免疫原:Synthetic Peptide
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免疫原种属:Homo sapiens (Human)
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标记方式:Non-conjugated
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纯化方式:The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using specific immunogen.
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浓度:It differs from different batches. Please contact us to confirm it.
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保存缓冲液:Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
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产品提供形式:Liquid
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应用范围:IHC,ELISA
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推荐稀释比:
Application Recommended Dilution IHC IHC-p:1:100-200 -
Protocols:
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储存条件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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货期: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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靶点详情
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功能:Regulatory subunit of Kv4/D (Shal)-type voltage-gated rapidly inactivating A-type potassium channels. Regulates channel density, inactivation kinetics and rate of recovery from inactivation in a calcium-dependent and isoform-specific manner. In vitro, modulates KCND1/Kv4.1 and KCND2/Kv4.2 currents. Increases the presence of KCND2 at the cell surface.
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基因功能参考文献:
- This is the first copy number variation association study of the KCNIP1 gene in Chinese population, and these data indicated that KCNIP1 might function as a type 2 diabetes-susceptibility gene whose dysregulation alters insulin production. PMID: 29491224
- Study shows that the VAPB-PTPIP51 tethers regulate autophagy and demonstrates that overexpression of VAPB or PTPIP51 to tighten endoplasmic reticulum-mitochondria contacts impairs, whereas small interfering RNA-mediated loss of VAPB or PTPIP51 to loosen contacts stimulates, autophagosome formation. PMID: 28132811
- the current study provides evidence that genetic variants of Kv accessory proteins may contribute to the susceptibility of Attention-deficit/hyperactivity disorder. PMID: 29176790
- These studies showed that a common copy number variation in KCNIP1 gene is a genetic predictor of atrial fibrillation risk possibly pointing to a functional pathway. PMID: 26831368
- KCNIP1 from copy number variations study might function as a type 2 diabetes susceptibility gene whose dysregulation alters insulin production. PMID: 24886904
- Protein aggregation due to nsSNP resulting in P56S VABP protein is associated with amyotrophic lateral sclerosis PMID: 24681403
- V234I-VAPB induces ubiquitin aggregation followed by cell death; proposed that V234I-VAPB exhibits the characteristics of amyotrophic lateral sclerosis in spite of not having the typical aggregation property of different mutations in various neurodegenerative diseases PMID: 24792378
- our findings suggest that KChIP1 interacts with Kv4.3 in interneurons at the stratum lacunosum-moleculare/radiatum junction PMID: 21129448
- X-ray crystallographic and small-angle X-ray scattering data that show that the KChIP1-Kv4.3 N-terminal cytoplasmic domain complex is a cross-shaped octamer bearing two principal interaction sites. PMID: 17057713
- EF-hands 3 and 4 of KChIP1 are functionally involved in a specific association with PS on the membrane PMID: 19550036
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亚细胞定位:Cell membrane; Peripheral membrane protein. Cytoplasm. Cell projection, dendrite.
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蛋白家族:Recoverin family
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组织特异性:Isoform 1 and isoform 2 are expressed in brain and kidney. Isoform 1 is also expressed in liver, pancreas, skeletal muscle, small intestine and testis. Isoform 2 is also expressed in lung, pancreas, leukocytes, prostate and thymus.
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数据库链接:
HGNC: 15521
OMIM: 604660
KEGG: hsa:30820
STRING: 9606.ENSP00000395323
UniGene: Hs.484111
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