SNAP91 抗体
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- 抗原 See all SNAP91 抗体
- SNAP91 (Synaptosomal-Associated Protein 91 (SNAP91))
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适用
- 人, 大鼠, 小鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This SNAP91 antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant protein of human CALM2
- 亚型
- IgG
- Top Product
- Discover our top product SNAP91 Primary Antibody
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- 应用备注
- WB 1:500 - 1:2000
- 限制
- 仅限研究用
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- 浓度
- 1 mg/mL
- 缓冲液
- Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3.
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- 抗原
- SNAP91 (Synaptosomal-Associated Protein 91 (SNAP91))
- 别名
- CALM (SNAP91 产品)
- 别名
- AP180 antibody, CALM antibody, Ap180 antibody, 91kDa antibody, F1-20 antibody, mKIAA0656 antibody, synaptosome associated protein 91 antibody, synaptosomal-associated protein, 91kDa homolog antibody, synaptosomal-associated protein 91 antibody, SNAP91 antibody, LOC100147907 antibody, Snap91 antibody
- 背景
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Synonyms: CALM 1,CALM 2,CALM 3,CALM,CALM,CALM1,CALM2,Calm3,CALML2,calmodulin 1 (phosphorylase kinase,delta),Calmodulin 2 (phosphorylase kinase,delta),Calmodulin 3 (phosphorylase kinase,delta),Calmodulin,CaM,CAM I,CAM1,CAM2,CAM3,CAMB,CAMC,CAMI,CAMII,CPVT4,DD132,FLJ99410,LP7057 protein,PHKD,PHKD2,PHKD3,phosphorylase kinase delta,phosphorylase kinase,delta subunit
Background: This gene is a member of the calmodulin gene family. There are three distinct calmodulin genes dispersed throughout the genome that encode the identical protein, but differ at the nucleotide level. Calmodulin is a calcium binding protein that plays a role in signaling pathways, cell cycle progression and proliferation. Several infants with severe forms of long-QT syndrome (LQTS) who displayed life-threatening ventricular arrhythmias together with delayed neurodevelopment and epilepsy were found to have mutations in either this gene or another member of the calmodulin gene family (PMID:23388215). Mutations in this gene have also been identified in patients with less severe forms of LQTS (PMID:24917665), while mutations in another calmodulin gene family member have been associated with catecholaminergic polymorphic ventricular tachycardia (CPVT)(PMID:23040497), a rare disorder thought to be the cause of a significant fraction of sudden cardiac deaths in young individuals. Pseudogenes of this gene are found on chromosomes 10, 13, and 17. Alternative splicing results in multiple transcript variants encoding different isoforms.
- 分子量
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Observed_MW: 15kDa
Calculated_MW: 17kDa
- 基因ID
- 801
- UniProt
- P62158
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