COMP (NM_000095) Human Tagged ORF Clone Lentiviral Particle
SKU
RC211080L1V
Lenti ORF particles, COMP (Myc-DDK tagged) - Human cartilage oligomeric matrix protein (COMP), 200ul, >10^7 TU/mL
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
---|---|
Tag | Myc-DDK |
Target Symbol | COMP |
Synonyms | CTS2; EDM1; EPD1; MED; PSACH; THBS5; TSP5 |
Vector | pLenti-C-Myc-DDK |
Mammalian Cell Selection | None |
Sequence Data |
ORF Nucleotide Sequence
The ORF insert of this clone is exactly the same as(RC211080).
|
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. |
Shipping | Dry Ice |
Reference Data | |
RefSeq | NM_000095.2 |
RefSeq Size | 2471 bp |
RefSeq ORF | 2274 bp |
Locus ID | 1311 |
UniProt ID | P49747 |
Cytogenetics | 19p13.11 |
Domains | EGF, EGF_CA, tsp_3 |
Protein Families | Druggable Genome, Secreted Protein |
Protein Pathways | ECM-receptor interaction, Focal adhesion, TGF-beta signaling pathway |
MW | 82.9 kDa |
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] |
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