CACNA2D3 Antibody
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货号:CSB-PA741101
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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.:Q8IZS8
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基因名:
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别名:CACNA2D3Voltage-dependent calcium channel subunit alpha-2/delta-3 antibody; Voltage-gated calcium channel subunit alpha-2/delta-3) [Cleaved into: Voltage-dependent calcium channel subunit alpha-2-3; Voltage-dependent calcium channel subunit delta-3] antibody
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宿主:Rabbit
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反应种属:Human,Mouse,Rat
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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:WB,ELISA
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推荐稀释比:
Application Recommended Dilution WB 1:1000-2000 -
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:The alpha-2/delta subunit of voltage-dependent calcium channels regulates calcium current density and activation/inactivation kinetics of the calcium channel. Acts as a regulatory subunit for P/Q-type calcium channel (CACNA1A), N-type (CACNA1B), L-type (CACNA1C OR CACNA1D) but not T-type (CACNA1G).
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基因功能参考文献:
- Nine of the 32 (28.1%) iCCA patients had gene mutations at chromosome 3p, totaling 11 mutations across five genes. Those included five (15.6%) BAP1 mutations, two each (6.3%) of CACNA2D3 and RASSF1 mutations, and one each (3.1%) of ATG7 and PLCD1 mutations. Six (18.8%) cases had concurrent loss of chromosome 3p and gene mutations. PMID: 29122566
- Findings demonstrate the tumor suppressive role of CACNA2D3 in gliomas. CACNA2D3 operates via Ca 2thorn signaling and the activation of non-canonical Wnt signaling to inhibit cell proliferation and motility and induce apoptosis. PMID: 27583705
- The risk of developing anaemia is increased in reproductive age women carriers of A allele of rs1868505 (CACNA2D3) and/or T allele of rs13194491 (HIST1H2BJ). PMID: 26460247
- CACNA2D3-mediated increase in intracellular calcium (Ca2+) can induce mitochondrial-mediated apoptosis. PMID: 23649311
- CACNA2D3 is a novel tumor suppressor gene responsible for the 3p21 deletion event that plays a critical suppressing role in the development and progression of esophageal squamous cell carcinoma. PMID: 23560067
- CACNA2D3 polymorphism rs1375515 plays important role in iron status and is associated with the levels of iron-related biomarkers, as well as with iron clinical phenotypes (normal, iron de fi cient and anaemic). PMID: 23324578
- Expression of CACNA2D3 mRNA is regulated in breast cancer cell lines by methylation in the CpG island located in the 5' regulatory region of the gene. PMID: 22644305
- High CACNA2D3 gene expression is assiciated with glioblastoma multiforme. PMID: 22395973
- In humans, study found single-nucleotide polymorphisms in alpha2delta3 that are associated with reduced acute heat pain sensitivity in healthy volunteers and chronic postsurgical back pain. PMID: 21074052
- did not detect submicroscopic deletion or duplication nor sequence alteration in either CACNA2D3 or WNT5A in ZLS-affected individuals PMID: 17937436
- Loss of CACNA2D3 expression through aberrant promoter hypermethylation may contribute to gastric carcinogenesis. PMID: 18588891
- This publication primarily discusses the alpha2/delta 4 subunit, but also contains cDNA data relating to the gene described in this record. PMID: 12181424
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亚细胞定位:Membrane; Single-pass type I membrane protein.
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蛋白家族:Calcium channel subunit alpha-2/delta family
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组织特异性:Only detected in brain. Not present in lung, testis, aorta, spleen, jejunum, ventricular muscle and kidney (at protein level). According to PubMed:11687876, it is brain-specific, while according to PubMed:11245980, it is widely expressed.
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数据库链接:
HGNC: 15460
OMIM: 606399
KEGG: hsa:55799
STRING: 9606.ENSP00000419101
UniGene: Hs.656687
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