EVX2 (NM_001080458) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC212735L3V
- LentiORF®
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Lenti ORF particles, EVX2 (Myc-DDK tagged) - Human even-skipped homeobox 2 (EVX2), 200ul, >10^7 TU/mL
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Specifications
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
Tag | Myc-DDK |
Symbol | EVX2 |
Synonyms | EVX-2 |
Mammalian Cell Selection | Puromycin |
Vector | pLenti-C-Myc-DDK-P2A-Puro |
ACCN | NM_001080458 |
ORF Size | 1428 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC212735).
|
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_001080458.1, NP_001073927.1 |
RefSeq Size | 1617 |
RefSeq ORF | 1431 |
Locus ID | 344191 |
MW | 47.6 kDa |
Gene Summary | This gene is located at the 5' end of the HOXD gene cluster on chromosome 2. The encoded protein is a homeobox transcription factor that is related to the protein encoded by the Drosophila even-skipped (eve) gene, a member of the pair-rule class of segmentation genes. A 117 kb microdeletion at the 5' end of the HOXD gene cluster, which includes this gene and the HOXD9-HOXD13 genes, causes synpolydactyly, a dominantly inherited disease resulting in limb malformation. [provided by RefSeq, Sep 2009] |
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