UBA1 (NM_153280) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC219513L2V

  • LentiORF®

Lenti ORF particles, UBA1 (mGFP-tagged) - Human ubiquitin-like modifier activating enzyme 1 (UBA1), transcript variant 2, 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP



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CNY 12,540.00


货期*
详询

规格
    • 200 ul

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Specifications

Product Data
Product Name UBA1 (NM_153280) Human Tagged ORF Clone Lentiviral Particle
Synonyms A1S9; A1S9T; A1ST; AMCX1; CFAP124; GXP1; POC20; SMAX2; UBA1A; UBE1; UBE1X; VEXAS
Vector pLenti-C-mGFP
ACCN NM_153280
ORF Size 3174 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC219513).
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_153280.1
RefSeq Size 3483 bp
RefSeq ORF 3177 bp
Locus ID 7317
Domains UBACT, ThiF
Protein Pathways Parkinson's disease, Ubiquitin mediated proteolysis
MW 117.7 kDa
Gene Summary The protein encoded by this gene catalyzes the first step in ubiquitin conjugation to mark cellular proteins for degradation. This gene complements an X-linked mouse temperature-sensitive defect in DNA synthesis, and thus may function in DNA repair. It is part of a gene cluster on chromosome Xp11.23. Alternatively spliced transcript variants that encode the same protein have been described. [provided by RefSeq, Jul 2008]
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.
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