PAX3 (NM_181460) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC215348L4V
- LentiORF®
-
Lenti ORF particles, PAX3 (mGFP-tagged)-Human paired box 3 (PAX3), transcript variant PAX3H, 200ul, >10^7 TU/mL
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Specifications
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
Tag | mGFP |
Symbol | PAX3 |
Synonyms | CDHS; HUP2; WS1; WS3 |
Mammalian Cell Selection | Puromycin |
Vector | pLenti-C-mGFP-P2A-Puro |
ACCN | NM_181460 |
ORF Size | 1221 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC215348).
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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_181460.1, NP_852125.1 |
RefSeq Size | 2923 bp |
RefSeq ORF | 1224 bp |
Locus ID | 5077 |
Cytogenetics | 2q36.1 |
Protein Families | Adult stem cells, Druggable Genome, Embryonic stem cells, ES Cell Differentiation/IPS, Transcription Factors |
MW | 45 kDa |
Gene Summary | 'This gene is a member of the paired box (PAX) family of transcription factors. Members of the PAX family typically contain a paired box domain and a paired-type homeodomain. These genes play critical roles during fetal development. Mutations in paired box gene 3 are associated with Waardenburg syndrome, craniofacial-deafness-hand syndrome, and alveolar rhabdomyosarcoma. The translocation t(2;13)(q35;q14), which represents a fusion between PAX3 and the forkhead gene, is a frequent finding in alveolar rhabdomyosarcoma. Alternative splicing results in transcripts encoding isoforms with different C-termini. [provided by RefSeq, Jul 2008]' |
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