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MYL2 Monoclonal Antibody

商品貨號： PLA004945

適應(yīng) 性： 人

￥600元

規(guī)格：

40μL 100μL 200μL

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MSDS

說明書

商品描述

發(fā)貨日期： 7
基因名稱： MYL2
蛋白名稱： Myosin regulatory light chain 2 ventricular/cardiac muscle isoform
Human_gene_id： 4633
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=4633
Human_swiss_prot_no： P10916
Human_swiss_link： http://www.uniprot.org/uniprotkb/P10916/entry
Mouse_swiss_prot_no： P51667
Mouse_swiss_link： http://www.uniprot.org/uniprot/P51667
特異性： MYL2 Monoclonal Antibody detects endogenous levels of MYL2 protein.
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來源： Monoclonal, Mouse
稀釋： WB 1:500 - 1:2000. ELISA: 1:10000. Not yet tested in other applications.
純化工藝： Affinity purification
儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
說明書： 1
Msds： MSDS_Antibody.pdf
其他名稱： MYL2; Myosin regulatory light chain 2; ventricular/cardiac muscle isoform; MLC-2; MLC-2v
信號通路： Cardiac muscle contraction;Focal adhesion;Tight junction;Leukocyte transendothelial migration;Regulates Actin and Cytoskeleton;Hypertrophic cardiomyopathy (HCM);Dilated cardiomyopathy;
功能： disease:Defects in MYL2 are the cause of cardiomyopathy familial hypertrophic type 10 (CMH10) [MIM:608758]. Familial hypertrophic cardiomyopathy is a hereditary heart disorder characterized by ventricular hypertrophy, which is usually asymmetric and often involves the interventricular septum. The symptoms include dyspnea, syncope, collapse, palpitations, and chest pain. They can be readily provoked by exercise. The disorder has inter- and intrafamilial variability ranging from benign to malignant forms with high risk of cardiac failure and sudden cardiac death.,disease:Defects in MYL2 are the cause of cardiomyopathy hypertrophic with mid-left ventricular chamber type 2 (MVC2) [MIM:608758]. MVC2 is a very rare variant of familial hypertrophic cardiomyopathy, characterized by mid-left ventricular chamber thickening.,miscellaneous:This chain binds calcium.,similarity:Contains 3 EF-hand domains.,subunit:Myosin is an hexamer of 2 heavy chains and 4 light chains.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細胞定位： Cytoplasm, myofibril, sarcomere, A band .
組織表達： Highly expressed in type I muscle fibers.
科研貨號： PLA004945

MYL2 Monoclonal Antibody

Catalog No PLA004945

Product information

發(fā)貨日期： 7
基因名稱： MYL2
蛋白名稱： Myosin regulatory light chain 2 ventricular/cardiac muscle isoform
Human_gene_id： 4633
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=4633
Human_swiss_prot_no： P10916
Human_swiss_link： http://www.uniprot.org/uniprotkb/P10916/entry
Mouse_swiss_prot_no： P51667
Mouse_swiss_link： http://www.uniprot.org/uniprot/P51667
特異性： MYL2 Monoclonal Antibody detects endogenous levels of MYL2 protein.
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來源： Monoclonal, Mouse
稀釋： WB 1:500 - 1:2000. ELISA: 1:10000. Not yet tested in other applications.
純化工藝： Affinity purification
儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
說明書： 1
Msds： MSDS_Antibody.pdf
其他名稱： MYL2; Myosin regulatory light chain 2; ventricular/cardiac muscle isoform; MLC-2; MLC-2v
信號通路： Cardiac muscle contraction;Focal adhesion;Tight junction;Leukocyte transendothelial migration;Regulates Actin and Cytoskeleton;Hypertrophic cardiomyopathy (HCM);Dilated cardiomyopathy;
功能： disease:Defects in MYL2 are the cause of cardiomyopathy familial hypertrophic type 10 (CMH10) [MIM:608758]. Familial hypertrophic cardiomyopathy is a hereditary heart disorder characterized by ventricular hypertrophy, which is usually asymmetric and often involves the interventricular septum. The symptoms include dyspnea, syncope, collapse, palpitations, and chest pain. They can be readily provoked by exercise. The disorder has inter- and intrafamilial variability ranging from benign to malignant forms with high risk of cardiac failure and sudden cardiac death.,disease:Defects in MYL2 are the cause of cardiomyopathy hypertrophic with mid-left ventricular chamber type 2 (MVC2) [MIM:608758]. MVC2 is a very rare variant of familial hypertrophic cardiomyopathy, characterized by mid-left ventricular chamber thickening.,miscellaneous:This chain binds calcium.,similarity:Contains 3 EF-hand domains.,subunit:Myosin is an hexamer of 2 heavy chains and 4 light chains.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細胞定位： Cytoplasm, myofibril, sarcomere, A band .
組織表達： Highly expressed in type I muscle fibers.
科研貨號： PLA004945

Hunan UPT Biotechnology Co.,Ltd

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