SREBP1 (SREBF1) (NM_004176) Human Tagged ORF Clone Lentiviral Particle

SKU RC208404L2V

Lenti ORF particles, SREBF1 (mGFP-tagged)-Human sterol regulatory element binding transcription factor 1 (SREBF1), transcript variant 2, 200ul, >10^7 TU/mL

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: mGFP
• Target Symbol: SREBP1
• Synonyms: bHLHd1; HMD; IFAP2; SREBP1
• Vector: pLenti-C-mGFP
• Mammalian Cell Selection: None
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC208404).
• ACCN: NM_004176
• ORF Size: 3441 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_004176.3
• RefSeq Size: 4922 bp
• RefSeq ORF: 3444 bp
• Locus ID: 6720
• UniProt ID: P36956
• Cytogenetics: 17p11.2
• Domains: HLH
• Protein Families: Druggable Genome, Transcription Factors
• Protein Pathways: Insulin signaling pathway
• MW: 122.2 kDa
• Summary: This gene encodes a basic helix-loop-helix-leucine zipper (bHLH-Zip) transcription factor that binds to the sterol regulatory element-1 (SRE1), which is a motif that is found in the promoter of the low density lipoprotein receptor gene and other genes involved in sterol biosynthesis. The encoded protein is synthesized as a precursor that is initially attached to the nuclear membrane and endoplasmic reticulum. Following cleavage, the mature protein translocates to the nucleus and activates transcription. This cleaveage is inhibited by sterols. This gene is located within the Smith-Magenis syndrome region on chromosome 17. Alternative promoter usage and splicing result in multiple transcript variants, including SREBP-1a and SREBP-1c, which correspond to RefSeq transcript variants 2 and 3, respectively. [provided by RefSeq, Nov 2017]