FOXP3 (NM_014009) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC217580L4V

Lenti ORF particles, FOXP3 (mGFP-tagged) - Human forkhead box P3 (FOXP3), transcript variant 1, 200ul, >10^7 TU/mL

Product Images

RC217580L4 was used to prepare Lentiviral particles using TR30037 packaging kit. HEK293T cells were transduced with RC217580L4V particle to overexpress human FOXP3-mGFP fusion protein.

• 

  RC217580L4 was used to prepare Lentiviral particles using TR30037 packaging kit. HEK293T cells were transduced with RC217580L4V particle to overexpress human FOXP3-mGFP fusion protein.

Specifications

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: mGFP
• Symbol: FOXP3
• Synonyms: AIID; DIETER; IPEX; JM2; PIDX; XPID
• Mammalian Cell Selection: Puromycin
• Vector: pLenti-C-mGFP-P2A-Puro
• ACCN: NM_014009
• ORF Size: 1293 bp
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC217580).
• 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_014009.2
• RefSeq Size: 1869 bp
• RefSeq ORF: 1296 bp
• Locus ID: 50943
• UniProt ID: Q9BZS1
• Cytogenetics: Xp11.23
• Protein Families: Transcription Factors
• MW: 47.1 kDa
• Gene Summary: The protein encoded by this gene is a member of the forkhead/winged-helix family of transcriptional regulators. Defects in this gene are the cause of immunodeficiency polyendocrinopathy, enteropathy, X-linked syndrome (IPEX), also known as X-linked autoimmunity-immunodeficiency syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]