Human PLN/CMD1P/CMH18 ORF/cDNA clone-Lentivirus plasmid (NM_002667)

Cat. No.: pGMLP000281
Size: 10 µg
Concentration: generally 0.5ug/ul, usually not less than 0.3ug/ul
Leading Time: 3-7 working days

Pre-made Human PLN/CMD1P/CMH18 Lentiviral expression plasmid for PLN lentivirus packaging, PLN lentivirus production, overexpression stable cell line development, cell transient transfection and gene delivery targeting T/B/NK cells, macrophages, cardiomyocytes, hepatocytes, and neurons.

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Product Description

Catalog ID pGMLP000281
Gene Name PLN
Accession Number NM_002667
Gene ID 5350
Species Human
Product Type Lentivirus plasmid (overexpression)
Insert Length 159 bp
Gene Alias CMD1P,CMH18,PLB
Fluorescent Reporter ZsGreen
Mammalian Cell Selection Puromyocin
Fusion Tag 3xflag (C-Terminal)
Promoter CMV
Resistance Amplicin
ORF Nucleotide Sequence ATGGAGAAAGTCCAATACCTCACTCGCTCAGCTATAAGAAGAGCCTCAACCATTGAAATGCCTCAACAAGCACGTCAAAAGCTACAGAATCTATTTATCAATTTCTGTCTCATCTTAATATGTCTCTTGCTGATCTGTATCATCGTGATGCTTCTCTGA
ORF Protein Sequence MEKVQYLTRSAIRRASTIEMPQQARQKLQNLFINFCLILICLLLICIIVMLL

Reference




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    Associated products


    Category Cat No. Products Name
    Target Antibody GM-Tg-g-IP0178-Ab Anti-PLN monoclonal antibody
    Target Antigen GM-Tg-g-IP0178-Ag PLN protein
    ORF Viral Vector pGMLP000281 Human PLN Lentivirus plasmid
    ORF Viral Vector vGMLP000281 Human PLN Lentivirus particle


    Target information

    Target ID GM-IP0178
    Target Name PLN
    Gene ID 5350, 18821, 100426104, 64672, 101097897, 414755, 100125240, 100630668
    Gene Symbol and Synonyms CMD1P,CMH18,PLB,Plm,PLN
    Uniprot Accession P26678
    Uniprot Entry Name PPLA_HUMAN
    Protein Sub-location Introcelluar Protein
    Category Therapeutics Target
    Disease Prostate Cancer
    Gene Ensembl ENSG00000198523
    Target Classification Not Available

    The protein encoded by this gene is found as a pentamer and is a major substrate for the cAMP-dependent protein kinase in cardiac muscle. The encoded protein is an inhibitor of cardiac muscle sarcoplasmic reticulum Ca(2+)-ATPase in the unphosphorylated state, but inhibition is relieved upon phosphorylation of the protein. The subsequent activation of the Ca(2+) pump leads to enhanced muscle relaxation rates, thereby contributing to the inotropic response elicited in heart by beta-agonists. The encoded protein is a key regulator of cardiac diastolic function. Mutations in this gene are a cause of inherited human dilated cardiomyopathy with refractory congestive heart failure, and also familial hypertrophic cardiomyopathy. [provided by RefSeq, Apr 2016]



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