Human MATN1/CMP/CRTM ORF/cDNA clone-Lentivirus plasmid (NM_002379)

Cat. No.: pGMLP001689
Size: 10 µg
Concentration: generally 0.5ug/ul, usually not less than 0.3ug/ul
Leading Time: 3-7 working days

Pre-made Human MATN1/CMP/CRTM Lentiviral expression plasmid for MATN1 lentivirus packaging, MATN1 lentivirus production, overexpression stable cell line development, cell transient transfection and gene delivery targeting T/B/NK cells, macrophages, cardiomyocytes, hepatocytes, and neurons.

Our GM-Lentiviral vector is seamlessly integrated with the GM lentivirus packaging system. Discover more about the GM lentivirus packaging system.

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Product Description

Catalog ID pGMLP001689
Gene Name MATN1
Accession Number NM_002379
Gene ID 4146
Species Human
Product Type Lentivirus plasmid (overexpression)
Insert Length 1491 bp
Gene Alias CMP,CRTM
Fluorescent Reporter ZsGreen
Mammalian Cell Selection Puromyocin
Fusion Tag 3xflag (C-Terminal)
Promoter CMV
Resistance Amplicin
ORF Nucleotide Sequence ATGAGGGTCCTCTCTGGCACTAGCCTCATGCTCTGCAGCCTGCTGCTGCTGCTCCAGGCCCTGTGCAGCCCTGGCCTCGCCCCCCAGTCCAGAGGCCATCTCTGCCGGACGCGGCCCACAGACCTGGTGTTTGTTGTCGACAGCTCTCGCAGCGTTCGGCCTGTTGAATTTGAGAAAGTGAAGGTATTCCTGTCCCAGGTCATCGAGTCGCTGGACGTGGGGCCCAATGCCACCCGGGTGGGCATGGTCAACTATGCCAGCACCGTGAAGCAGGAGTTCTCGCTGCGGGCTCATGTCTCCAAGGCCGCACTGCTGCAGGCTGTGCGCCGTATCCAGCCGCTGTCCACAGGCACCATGACCGGCCTGGCCATCCAGTTCGCTATCACCAAAGCCTTCGGCGATGCAGAGGGTGGTCGTTCCAGGTCCCCTGACATCAGCAAGGTGGTCATCGTGGTGACAGACGGGAGGCCCCAGGACAGCGTGCAGGACGTGTCTGCGCGGGCCCGGGCCAGCGGCGTCGAGCTGTTCGCCATCGGAGTGGGCAGCGTGGACAAGGCCACGCTGCGGCAGATCGCCAGCGAGCCGCAGGACGAACACGTCGATTACGTGGAGAGCTACAGCGTCATCGAGAAGCTGTCCAGGAAGTTCCAGGAGGCCTTCTGCGTGGTGTCAGACCTGTGCGCCACAGGGGACCATGACTGTGAGCAGGTGTGCATCAGCTCCCCCGGTTCCTACACCTGCGCCTGCCACGAGGGCTTCACTCTGAACAGCGACGGCAAGACCTGCAATGTCTGCAGTGGTGGTGGTGGCAGCTCGGCCACTGACCTGGTCTTCCTCATTGACGGATCCAAGAGTGTGAGGCCAGAGAACTTTGAGCTGGTGAAGAAGTTCATCAGTCAGATCGTGGATACGCTGGACGTGTCAGACAAGCTGGCCCAGGTGGGGCTGGTGCAGTACTCAAGCTCTGTGCGCCAGGAGTTCCCCCTGGGTCGCTTCCACACCAAGAAGGACATCAAGGCGGCTGTGCGGAATATGTCCTACATGGAGAAGGGCACAATGACTGGGGCTGCTCTCAAGTACCTCATTGACAATTCCTTCACTGTGTCCAGTGGGGCTAGGCCCGGGGCCCAGAAGGTGGGCATTGTCTTCACTGATGGCCGGAGCCAGGACTACATTAATGATGCTGCCAAGAAGGCCAAAGACCTCGGCTTTAAGATGTTTGCTGTGGGTGTGGGCAATGCCGTGGAGGATGAGCTGAGGGAAATAGCCTCAGAGCCTGTGGCAGAGCACTACTTCTACACGGCTGACTTCAAGACCATCAACCAGATAGGCAAGAAGTTGCAGAAGAAGATCTGTGTGGAGGAAGACCCGTGTGCCTGCGAGTCCCTGGTGAAATTCCAAGCCAAAGTGGAGGGGCTGCTGCAGGCCCTGACCAGGAAACTGGAAGCTGTGAGTAAGCGGCTGGCCATCCTGGAGAACACAGTTGTCTAA
ORF Protein Sequence MRVLSGTSLMLCSLLLLLQALCSPGLAPQSRGHLCRTRPTDLVFVVDSSRSVRPVEFEKVKVFLSQVIESLDVGPNATRVGMVNYASTVKQEFSLRAHVSKAALLQAVRRIQPLSTGTMTGLAIQFAITKAFGDAEGGRSRSPDISKVVIVVTDGRPQDSVQDVSARARASGVELFAIGVGSVDKATLRQIASEPQDEHVDYVESYSVIEKLSRKFQEAFCVVSDLCATGDHDCEQVCISSPGSYTCACHEGFTLNSDGKTCNVCSGGGGSSATDLVFLIDGSKSVRPENFELVKKFISQIVDTLDVSDKLAQVGLVQYSSSVRQEFPLGRFHTKKDIKAAVRNMSYMEKGTMTGAALKYLIDNSFTVSSGARPGAQKVGIVFTDGRSQDYINDAAKKAKDLGFKMFAVGVGNAVEDELREIASEPVAEHYFYTADFKTINQIGKKLQKKICVEEDPCACESLVKFQAKVEGLLQALTRKLEAVSKRLAILENTVV

Reference




    Data / case study


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    Associated products


    Category Cat No. Products Name
    Target Antibody GM-Tg-g-SE1090-Ab Anti-MATN1/ CMP/ CRTM functional antibody
    Target Antigen GM-Tg-g-SE1090-Ag MATN1 protein
    ORF Viral Vector pGMLP001689 Human MATN1 Lentivirus plasmid
    ORF Viral Vector vGMLP001689 Human MATN1 Lentivirus particle


    Target information

    Target ID GM-SE1090
    Target Name MATN1
    Gene ID 4146, 17180, 704521, 297894, 101092626, 487325, 512059, 100056375
    Gene Symbol and Synonyms CMP,CRTM,Mat1,MATN1,matrilin-1
    Uniprot Accession P21941
    Uniprot Entry Name MATN1_HUMAN
    Protein Sub-location Secreted Protein/Potential Cytokines
    Category Not Available
    Disease Not Available
    Gene Ensembl ENSG00000162510
    Target Classification Not Available

    This gene encodes a member of von Willebrand factor A domain containing protein family. This family of proteins are thought to be involved in the formation of filamentous networks in the extracellular matrices of various tissues. Mutations of this gene have been associated with variety of inherited chondrodysplasias. [provided by RefSeq, Jul 2008]



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