Dystrobrevin alpha (DTNA) (NM_032979) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC223952L4V

  • LentiORF®

Lenti ORF particles, DTNA (mGFP-tagged) - Human dystrobrevin, alpha (DTNA), transcript variant 5, 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP

Lentiviral Particles: DDK w/ Puro mGFP w/ Puro

AAV Particle: DDK


Buy this product and get 50% off on the Lenti RapidTiter kit. Use Code: Rapid50

USD 1,028.00

7 Weeks*

Size
    • 200 ul

Product Images

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Specifications

Product Data
Type Human Tagged ORF Clone Lentiviral Particle
Tag mGFP
Symbol Dystrobrevin alpha
Synonyms D18S892E; DRP3; DTN; DTN-A; LVNC1
Mammalian Cell Selection Puromycin
Vector pLenti-C-mGFP-P2A-Puro
ACCN NM_032979
ORF Size 1539 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC223952).
OTI Disclaimer The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info
OTI Annotation This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene.
Reference Data
RefSeq NM_032979.2
RefSeq Size 3110 bp
RefSeq ORF 1542 bp
Locus ID 1837
UniProt ID Q9Y4J8
Cytogenetics 18q12.1
Domains ZnF_ZZ
Protein Families Druggable Genome
MW 58.7 kDa
Gene Summary The protein encoded by this gene belongs to the dystrobrevin subfamily of the dystrophin family. This protein is a component of the dystrophin-associated protein complex (DPC), which consists of dystrophin and several integral and peripheral membrane proteins, including dystroglycans, sarcoglycans, syntrophins and alpha- and beta-dystrobrevin. The DPC localizes to the sarcolemma and its disruption is associated with various forms of muscular dystrophy. Mutations in this gene are associated with left ventricular noncompaction with congenital heart defects. Multiple alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]

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