Alpha Fodrin (SPTAN1) (NM_001130438) Human Tagged ORF Clone Lentiviral Particle

SKU
RC226485L1V
Lenti ORF particles, SPTAN1 (Myc-DDK tagged) - Human spectrin, alpha, non-erythrocytic 1 (alpha-fodrin) (SPTAN1), transcript variant 1, 200ul, >10^7 TU/mL
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$2,594.00
3 Weeks*
Specifications
Product Data
Type Human Tagged ORF Clone Lentiviral Particle
Tag Myc-DDK
Target Symbol Alpha Fodrin
Synonyms DEE5; EIEE5; NEAS; SPTA2
Vector pLenti-C-Myc-DDK
Mammalian Cell Selection None
Sequence Data
ORF Nucleotide Sequence
The ORF insert of this clone is exactly the same as(RC226485).
ACCN NM_001130438
ORF Size 7431 bp
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.
Shipping Dry Ice
Reference Data
RefSeq NM_001130438.2, NP_001123910.1
RefSeq Size 7907 bp
RefSeq ORF 7434 bp
Locus ID 6709
UniProt ID Q13813
Cytogenetics 9q34.11
Protein Families Druggable Genome
Protein Pathways Tight junction
MW 285.5 kDa
Summary Spectrins are a family of filamentous cytoskeletal proteins that function as essential scaffold proteins that stabilize the plasma membrane and organize intracellular organelles. Spectrins are composed of alpha and beta dimers that associate to form tetramers linked in a head-to-head arrangement. This gene encodes an alpha spectrin that is specifically expressed in nonerythrocytic cells. The encoded protein has been implicated in other cellular functions including DNA repair and cell cycle regulation. Mutations in this gene are the cause of early infantile epileptic encephalopathy-5. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Sep 2010]
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