首页 > 抗体 > 一抗 > 其它 > DTNA rabbit pAb
DTNA rabbit pAb
商品货号: PLA019857
适 应 性: 人,小鼠
WB
¥600元
规格:
在线咨询
MSDS
说明书
商品描述
  • 基因名称: DTNA DRP3
  • 蛋白名称: DTNA
  • Human_gene_id: 1837
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=1837
  • Human_swiss_prot_no: Q9Y4J8
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/Q9Y4J8/entry
  • Mouse_gene_id: 13527
  • Mouse_gene_link: https://www.uniprot.org/uniprot/13527
  • Mouse_swiss_prot_no: Q9D2N4
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/Q9D2N4
  • 特异性: This antibody detects endogenous levels of DTNA at Human/Mouse
  • 组成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 来源: Polyclonal, Rabbit,IgG
  • 稀释: WB 1:500-2000
  • 纯化工艺: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 浓度: 1 mg/ml
  • 储存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 说明书: 1
  • Msds: MSDS_Antibody.pdf
  • 分子量: 82kD
  • 功能: alternative products:Additional isoforms seem to exist,disease:Defects in DTNA are a cause of non-compaction of left ventricular myocardium with congenital heart defects (LVNCCHD) [MIM:606617]; also known as non-isolated left ventricular non-compaction. LVNCCHD is associated with congenital heart anomalies such as ventricular septal defects, pulmonic stenosis, and atrial septal defects.,disease:Defects in DTNA are the cause of non-compaction of left ventricular myocardium isolated autosomal dominant type 1 (LVNC1) [MIM:604169]. Left ventricular non-compaction (LVNC) is due to an arrest of myocardial morphogenesis. The disorder is characterized by a hypertrophic left ventricular with deep trabeculations and with poor systolic function, with or without associated left ventricular dilation. In some cases, the right ventricle is also affected.,domain:The coiled coil domain mediates the interaction with dystrophin and utrophin.,function:May be involved in the formation and stability of synapses as well as being involved in the clustering of nicotinic acetylcholine receptors.,PTM:Phosphorylation of DTN-1 on tyrosine kinase substrate domain present in the C-terminus.,similarity:Belongs to the dystrophin family. Dystrobrevin subfamily.,similarity:Contains 1 ZZ-type zinc finger.,subunit:Interacts with dystrophin, utrophin and the syntrophins SNTA1, SNTB1, SNTB2, SNTG1 and SNTG2. Isoforms 7 and 8 do not interact with dystrophin. Binds dystrobrevin binding protein 1.,tissue specificity:Highly expressed in brain, skeletal and cardiac muscles, and expressed at lower levels in lung, liver and pancreas. Isoform 2 is not expressed in cardiac muscle. Isoforms 7 and 8 are only expressed in muscle.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Cytoplasm. Cell junction, synapse. Cell membrane . In peripheral nerves, colocalizes with MAGEE1 in the Schwann cell membrane. .
  • 组织表达: Highly expressed in brain, skeletal and cardiac muscles, and expressed at lower levels in lung, liver and pancreas. Isoform 2 is not expressed in cardiac muscle. Isoform 7 and isoform 8 are only expressed in muscle.
  • 科研货号: PLA019857
DTNA rabbit pAb
Catalog No PLA019857
Product information
  • 基因名称: DTNA DRP3
  • 蛋白名称: DTNA
  • Human_gene_id: 1837
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=1837
  • Human_swiss_prot_no: Q9Y4J8
  • Human_swiss_link: https://www.uniprot.org/uniprotkb/Q9Y4J8/entry
  • Mouse_gene_id: 13527
  • Mouse_gene_link: https://www.uniprot.org/uniprot/13527
  • Mouse_swiss_prot_no: Q9D2N4
  • Mouse_swiss_link: https://www.uniprot.org/uniprotkb/Q9D2N4
  • 特异性: This antibody detects endogenous levels of DTNA at Human/Mouse
  • 组成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 来源: Polyclonal, Rabbit,IgG
  • 稀释: WB 1:500-2000
  • 纯化工艺: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 浓度: 1 mg/ml
  • 储存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 说明书: 1
  • Msds: MSDS_Antibody.pdf
  • 分子量: 82kD
  • 功能: alternative products:Additional isoforms seem to exist,disease:Defects in DTNA are a cause of non-compaction of left ventricular myocardium with congenital heart defects (LVNCCHD) [MIM:606617]; also known as non-isolated left ventricular non-compaction. LVNCCHD is associated with congenital heart anomalies such as ventricular septal defects, pulmonic stenosis, and atrial septal defects.,disease:Defects in DTNA are the cause of non-compaction of left ventricular myocardium isolated autosomal dominant type 1 (LVNC1) [MIM:604169]. Left ventricular non-compaction (LVNC) is due to an arrest of myocardial morphogenesis. The disorder is characterized by a hypertrophic left ventricular with deep trabeculations and with poor systolic function, with or without associated left ventricular dilation. In some cases, the right ventricle is also affected.,domain:The coiled coil domain mediates the interaction with dystrophin and utrophin.,function:May be involved in the formation and stability of synapses as well as being involved in the clustering of nicotinic acetylcholine receptors.,PTM:Phosphorylation of DTN-1 on tyrosine kinase substrate domain present in the C-terminus.,similarity:Belongs to the dystrophin family. Dystrobrevin subfamily.,similarity:Contains 1 ZZ-type zinc finger.,subunit:Interacts with dystrophin, utrophin and the syntrophins SNTA1, SNTB1, SNTB2, SNTG1 and SNTG2. Isoforms 7 and 8 do not interact with dystrophin. Binds dystrobrevin binding protein 1.,tissue specificity:Highly expressed in brain, skeletal and cardiac muscles, and expressed at lower levels in lung, liver and pancreas. Isoform 2 is not expressed in cardiac muscle. Isoforms 7 and 8 are only expressed in muscle.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Cytoplasm. Cell junction, synapse. Cell membrane . In peripheral nerves, colocalizes with MAGEE1 in the Schwann cell membrane. .
  • 组织表达: Highly expressed in brain, skeletal and cardiac muscles, and expressed at lower levels in lung, liver and pancreas. Isoform 2 is not expressed in cardiac muscle. Isoform 7 and isoform 8 are only expressed in muscle.
  • 科研货号: PLA019857
  • Hunan UPT Biotechnology Co.,Ltd
    Website:www.uptbio.com Servive hotline :4006916686
    E-mail:service@uptbio.com
    Address:
    Room 402, Building 13, Xinggong International Industrial Park, 100 Guyuan Road, Yuelu District, Changsha City, Hunan Province, China.
普拉特泽实验室电话助手

4006916686

扫码咨询