MUM1 (IRF4) (NM_002460) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC204876L2V

  • LentiORF®

Lenti ORF particles, IRF4 (mGFP-tagged) - Human interferon regulatory factor 4 (IRF4), transcript variant 1, 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP

Lentiviral Particles: DDK DDK w/ Puro mGFP mGFP w/ Puro


Special Offer: Buy this product and get 50% off Lenti Control Particles. Learn More.

USD 1,236.00

2 Weeks*

Size
    • 200 ul

Product Images

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Specifications

Product Data
Type Human Tagged ORF Clone Lentiviral Particle
Tag mGFP
Symbol MUM1
Synonyms LSIRF; MUM1; NF-EM5; SHEP8
Mammalian Cell Selection None
Vector pLenti-C-mGFP
ACCN NM_002460
ORF Size 1353 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC204876).
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_002460.1
RefSeq Size 5332 bp
RefSeq ORF 1356 bp
Locus ID 3662
UniProt ID Q15306
Cytogenetics 6p25.3
Protein Families Druggable Genome, Transcription Factors
MW 51.8 kDa
Gene Summary The protein encoded by this gene belongs to the IRF (interferon regulatory factor) family of transcription factors, characterized by an unique tryptophan pentad repeat DNA-binding domain. The IRFs are important in the regulation of interferons in response to infection by virus, and in the regulation of interferon-inducible genes. This family member is lymphocyte specific and negatively regulates Toll-like-receptor (TLR) signaling that is central to the activation of innate and adaptive immune systems. A chromosomal translocation involving this gene and the IgH locus, t(6;14)(p25;q32), may be a cause of multiple myeloma. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2010]

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*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.