Human NEU1/NANH/NEU ORF/cDNA clone-Lentivirus plasmid (NM_000434.4)

SKU: pGMLV002700
Size: 10 µg
Concentration: generally 0.5ug/ul, usually not less than 0.3ug/ul
Leading Time: 3-7 working days

Pre-made Human NEU1/NANH/NEU Lentiviral expression plasmid for NEU1 lentivirus packaging, NEU1 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 pGMLV002700
Gene Name NEU1
Accession Number NM_000434.4
Gene ID 4758
Species Human
Product Type Lentivirus plasmid (overexpression)
Insert Length 1248 bp
Gene Alias NANH,NEU,SIAL1
Fluorescent Reporter ZsGreen
Mammalian Cell Selection Puromyocin
Fusion Tag 3xflag (C-Terminal)
Promoter CMV
Resistance Amplicin
Sequence ATGACTGGGGAGCGACCCAGCACGGCGCTCCCGGACAGACGCTGGGGGCCGCGGATTCTGGGCTTCTGGGGAGGCTGTAGGGTTTGGGTGTTTGCCGCGATCTTCCTGCTGCTGTCTCTGGCAGCCTCCTGGTCCAAGGCTGAGAACGACTTCGGTCTGGTGCAGCCGCTGGTGACCATGGAGCAACTGCTGTGGGTGAGCGGGAGACAGATCGGCTCAGTGGACACCTTCCGCATCCCGCTCATCACAGCCACTCCGCGGGGCACTCTTCTCGCCTTTGCTGAGGCGAGGAAAATGTCCTCATCCGATGAGGGGGCCAAGTTCATCGCCCTGCGGAGGTCCATGGACCAGGGCAGCACATGGTCTCCTACAGCGTTCATTGTCAATGATGGGGATGTCCCCGATGGGCTGAACCTTGGGGCAGTAGTGAGCGATGTTGAGACAGGAGTAGTATTTCTTTTCTACTCCCTTTGTGCTCACAAGGCCGGCTGCCAGGTGGCCTCTACCATGTTGGTATGGAGCAAGGATGATGGTGTTTCCTGGAGCACACCCCGGAATCTCTCCCTGGATATTGGCACTGAAGTGTTTGCCCCTGGACCGGGCTCTGGTATTCAGAAACAGCGGGAGCCACGGAAGGGCCGCCTCATCGTGTGTGGCCATGGGACGCTGGAGCGGGACGGAGTCTTCTGTCTCCTCAGCGATGATCATGGTGCCTCCTGGCGCTACGGAAGTGGGGTCAGCGGCATCCCCTACGGTCAGCCCAAGCAGGAAAATGATTTCAATCCTGATGAATGCCAGCCCTATGAGCTCCCAGATGGCTCAGTCGTCATCAATGCCCGAAACCAGAACAACTACCACTGCCACTGCCGAATTGTCCTCCGCAGCTATGATGCCTGTGATACACTAAGGCCCCGTGATGTGACCTTCGACCCTGAGCTCGTGGACCCTGTGGTAGCTGCAGGAGCTGTAGTCACCAGCTCCGGCATTGTCTTCTTCTCCAACCCAGCACATCCAGAGTTCCGAGTGAACCTGACCCTGCGATGGAGCTTCAGCAATGGTACCTCATGGCGGAAAGAGACAGTCCAGCTATGGCCAGGCCCCAGTGGCTATTCATCCCTGGCAACCCTGGAGGGCAGCATGGATGGAGAGGAGCAGGCCCCCCAGCTCTACGTCCTGTATGAGAAAGGCCGGAACCACTACACAGAGAGCATCTCCGTGGCCAAAATCAGTGTCTATGGGACACTCTGA

Reference




    Data / case study


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    Associated products


    Category Cat No. Products Name
    Target Antibody GM-Tg-g-MP0874-Ab Anti-NEUR1/ NEU1/ NANH monoclonal antibody
    Target Antigen GM-Tg-g-MP0874-Ag NEU1 VLP (virus-like particle)
    ORF Viral Vector pGMLV002700 Human NEU1 Lentivirus plasmid
    ORF Viral Vector pGMAAV000260 Human NEU1 Adeno-associate virus(AAV) plasmid
    ORF Viral Vector pGMAAV000796 Human NEU1 Adeno-associate virus(AAV) plasmid
    ORF Viral Vector pGMAAV001253 Human NEU1 Adeno-associate virus(AAV) plasmid
    ORF Viral Vector pGMAP000094 Human NEU1 Adenovirus plasmid
    ORF Viral Vector pGMPC001869 Human NEU1 Mammalian (Non-Viral Vector) plasmid
    ORF Viral Vector vGMLV002700 Human NEU1 Lentivirus particle
    ORF Viral Vector vGMAAV000260 Human NEU1 Adeno-associate virus(AAV) particle
    ORF Viral Vector vGMAAV000796 Human NEU1 Adeno-associate virus(AAV) particle
    ORF Viral Vector vGMAAV001253 Human NEU1 Adeno-associate virus(AAV) particle
    ORF Viral Vector vGMAP000094 Human NEU1 Adenovirus particle


    Target information

    Target ID GM-MP0874
    Target Name NEU1
    Gene ID 4758, 18010, 716740, 24591, 101091282, 481717, 505554, 100059083
    Gene Symbol and Synonyms Aglp,Apl,Bat-7,Bat7,G9,Map-2,NANH,NEU,Neu-1,NEU1,SIAL1
    Uniprot Accession Q99519
    Uniprot Entry Name NEUR1_HUMAN
    Protein Sub-location Transmembrane Protein
    Category Not Available
    Disease Not Available
    Gene Ensembl ENSG00000204386
    Target Classification Not Available

    The protein encoded by this gene is a lysosomal enzyme that cleaves terminal sialic acid residues from substrates such as glycoproteins and glycolipids. In the lysosome, this enzyme is part of a heterotrimeric complex together with beta-galactosidase and cathepsin A (the latter is also referred to as 'protective protein'). Mutations in this gene can lead to sialidosis, a lysosomal storage disease that can be type 1 (cherry red spot-myoclonus syndrome or normosomatic type), which is late-onset, or type 2 (the dysmorphic type), which occurs at an earlier age with increased severity. [provided by RefSeq, Jul 2008]



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