ACTA1 Lentiviral Vector (Human) (CMV) (pLenti-GIII-CMV-RFP-2A-Puro)

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Catalog number: LV067755
Price: 322 €
Supplier: ABM lentivectors
Product name: ACTA1 Lentiviral Vector (Human) (CMV) (pLenti-GIII-CMV-RFP-2A-Puro)
Quantity: 1.0 µg DNA
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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: ACTA1 Lentiviral Vector (CMV) (pLenti-GIII-CMV-RFP-2A-Puro)
Short name: ACTA1 Lentiviral Vector ( ) (CMV) (pLenti-GIII-CMV-RFP-2A-Puro)
Technique: Vectors
Species: Humans, Human
Alternative name: sapiens) (cytomegalovirus) (pLenti-GIII-cytomegalovirus-Red Fluorescent-2A-Puro), ACTA1 Lentiviral integrating Desoxyribonucleic acid sequence (H
Identity: 129
Gene: ACTA1 | More about : ACTA1
Long gene name: actin, alpha 1, skeletal muscle
Synonyms gene: ACTA
Synonyms: NEM3
Synonyms name: nemaline myopathy type 3
Locus: 1q42, 13
Discovery year: 1986-01-01
GenBank acession: J00068
Entrez gene record: 58
Pubmed identfication: 10072583 6865942
RefSeq identity: NM_001100
Classification: Actins
Havana BLAST/BLAT: OTTHUMG00000038006
Locus Specific Databases: Leiden Muscular Dystrophy pages LRG_429

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