COMP (NM_000095) Human Tagged ORF Clone

CAT#: RC211080L2

Lenti ORF clone of Human cartilage oligomeric matrix protein (COMP), mGFP tagged

Specifications

Product Data

• Product Name: COMP (NM_000095) Human Tagged ORF Clone
• Symbol: COMP
• Synonyms: EDM1; EPD1; MED; PSACH; THBS5
• Vector: pLenti-C-mGFP
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC211080).
• Restriction Sites: SgfI-RsrII Cloning Scheme for this gene
• Tag: mGFP
• ACCN: NM_000095
• ORF Size: 2271 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.
• Product Components: The ORF clone is ion-exchange column purified, transfection-ready dried plasmid DNA, and shipped with 2 vector sequencing primers.

Reference Data

• RefSeq: NM_000095.2, NP_000086
• RefSeq Size: 2471
• RefSeq ORF: 2274
• Locus ID: 1311
• Cytogenetics: 19p13.11
• Domains: EGF_CA, tsp_3, EGF, EGF
• Protein Families: Secreted Protein, Druggable Genome
• Protein Pathways: TGF-beta signaling pathway, Focal adhesion, ECM-receptor interaction
• MW: 82.86 kDa
• Gene Summary: The protein encoded by this gene is a noncollagenous extracellular matrix (ECM) protein. It consists of five identical glycoprotein subunits, each with EGF-like and calcium-binding (thrombospondin-like) domains. Oligomerization results from formation of a five-stranded coiled coil and disulfides. Binding to other ECM proteins such as collagen appears to depend on divalent cations. Contraction or expansion of a 5 aa aspartate repeat and other mutations can cause pseudochondroplasia (PSACH) and multiple epiphyseal dysplasia (MED). [provided by RefSeq, Jul 2016]