TPP1 Lentiviral Vector (Human) (CMV) (pLenti-GIII-CMV)

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Catalog number: LV342683
Price: 2045 €
Supplier: MBS Recombinant Proteins
Product name: TPP1 Lentiviral Vector (Human) (CMV) (pLenti-GIII-CMV)
Quantity: 100ug
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DNA lentivector for transduction information: GENTAUR suggests to use our ABM packaging mix LV003 of second generation virusses or the LV053, This DNA can alos be used for packaging into Lentiviral particles for high efficiency transduction and stably integrated expressions, Vectors with selection markers like kanamycin, our 3rd Generation Packaging mixture, pLenti lentiviral plasmids DNAs are stored in 10milliMolar Tris/HCI with 1mM EDTA at a pH of 8 at -25 C, puromycin or cumate are available, Lentiveral packaging plasmid DNA for non-viral plasmid transfection and direct use in plasmid expression
Properties: Depending on the epitopes used human ELISA kits can be cross reactive to many other species, Mainly analyzed are human serum, Modern , cDNA and human recombinants are used in human reactive ELISA kits and to produce anti-human mono and polyclonal antibodies, human cell culture supernatants and biological samples, plasma, primarily , saliva, urine,  , (Homo sapiens, Homo sapiens sapiens), Human proteins, humans , ssp
Gene target: TPP1 Lentiviral Vector (CMV) (pLenti-GIII-CMV)
Short name: TPP1 Lentiviral Vector ( ) (CMV) (pLenti-GIII-CMV)
Technique: Vectors
Species: Humans, Human
Alternative name: sapiens) (cytomegalovirus) (pLenti-GIII-cytomegalovirus), TPP1 Lentiviral integrating Desoxyribonucleic acid sequence (H
Identity: 2073
Gene: TPP1 | More about : TPP1
Long gene name: tripeptidyl peptidase 1
Synonyms gene: CLN2 SCAR7
Synonyms gene name: autosomal recessive 7 tripeptidyl peptidase I , ceroid-lipofuscinosis, late infantile (Jansky-Bielschowsky disease) spinocerebellar ataxia, neuronal 2
Synonyms name: TPP I
Locus: 11p15, 4
Discovery year: 1990-01-30
GenBank acession: AF017456
Entrez gene record: 1200
Pubmed identfication: 9653647 23418007
Havana BLAST/BLAT: OTTHUMG00000133404
Locus Specific Databases: NCL Mutations LRG_830 , Neuronal Ceroid Lipofuscinoses

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