MSX1 (NM_002448) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC205682L2V

Lenti ORF particles, MSX1 (mGFP-tagged) - Human msh homeobox 1 (MSX1), 200ul, >10^7 TU/mL

Specifications

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: mGFP
• Symbol: MSX1
• Synonyms: ECTD3; HOX7; HYD1; STHAG1
• Mammalian Cell Selection: None
• Vector: pLenti-C-mGFP
• ACCN: NM_002448
• ORF Size: 909 bp
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC205682).
• 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_002448.3, NP_002439.2
• RefSeq Size: 1940 bp
• RefSeq ORF: 912 bp
• Locus ID: 4487
• UniProt ID: P28360
• Cytogenetics: 4p16.2
• Domains: homeobox
• Protein Families: Druggable Genome, Transcription Factors
• MW: 31.5 kDa
• Gene Summary: This gene encodes a member of the muscle segment homeobox gene family. The encoded protein functions as a transcriptional repressor during embryogenesis through interactions with components of the core transcription complex and other homeoproteins. It may also have roles in limb-pattern formation, craniofacial development, particularly odontogenesis, and tumor growth inhibition. Mutations in this gene, which was once known as homeobox 7, have been associated with nonsyndromic cleft lip with or without cleft palate 5, Witkop syndrome, Wolf-Hirschom syndrome, and autosomoal dominant hypodontia. [provided by RefSeq, Jul 2008]