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脊髓小脑共济失调2型蛋白抗体

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产物名称: 脊髓小脑共济失调2型蛋白抗体
产物型号: ATX2
产物展商: 单克隆抗体/多克隆抗体
产物文档: 无相关文档

简单介绍

脊髓小脑共济失调2型蛋白抗体应用于IHC、WB、 IF、IP、ELISA等科研实验,按理化性质和生物学功能IgM、IgG、IgA、IgE、IgD五类。按抗体的来源,可将其分为天然抗体和**抗体。脊髓小脑共济失调2型蛋白抗体生产每个流程都执行严格的检测标准,保证蛋白抗原产物质量,质量稳定,实验效果明显。


脊髓小脑共济失调2型蛋白抗体  的详细介绍

脊髓小脑共济失调2型蛋白抗体

规格:1尘驳/1尘濒

英文名: ATX2

别名: Ataxin 2; ATXN2; Olivopontocerebellar ataxia 2, autosomal dominant; SCA2; Spinocerebellar ataxia type 2 protein; TNRC13; Trinucleotide repeat containing gene 13 protein; SRRT_HUMAN.

分子量: 101kDa

储存液:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glyce

克隆类型:笔辞濒测肠濒辞苍补濒

亚型:滨驳骋

纯化方法:affinity purified by Protein A

**原:KLH conjugated synthetic peptide derived from human ATX2 (77

交叉反应:Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Horse,

细胞定位:细胞浆

脊髓小脑共济失调2型蛋白抗体产物介绍:background: The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ATX2 belongs to the autosomal dominant cerebellar ataxias type I (ADCA I) which are characterized by cerebellar ataxia in combination with additional clinical features like optic atrophy, ophthalmoplegia, bulbar and extrapyramidal signs, peripheral neuropathy and dementia. ATX2 is caused by expansion of a CAG repeat in the coding region of ATX2. Longer expansions result in earlier onset of the disease. There are four named isoforms. Subunit: Monomer. Can also form homodimers. Subcellular Location:脊髓小脑共济失调2型蛋白抗体 Cytoplasm. Tissue Specificity: Expressed in the brain, heart, liver, skeletal muscle, pancreas and placenta. Isoform 1 is predominant in the brain and spinal cord. Isoform 4 is more abundant in the cerebellum. In the brain, broadly expressed in the amygdala, caudate nucleus, corpus callosum, hippocampus, hypothalamus, substantia nigra, subthalamic nucleus and thalamus. Similarity: Belongs to the ataxin-2 family. Database links: Entrez Gene: 6311 Human Entrez Gene: 20239 Mouse Entrez Gene: 288663 Rat Omim: 601517 Human SwissProt: Q99700 Human 脊髓小脑共济失调2型蛋白抗体SwissProt: O70305 Mouse Unigene: 76253 Human Unigene: 260900 Mouse Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

脊髓小脑共济失调2型蛋白抗体产物应用:WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500 (石蜡切片需做抗原修复) not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.

研究领域:细胞生物  **学  神经生物学  表观遗传学  

储存条件: Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

来源: Rabbit

外观: Lyophilized or Liquid


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