MNX1 (NM_005515) Human Tagged ORF Clone Lentiviral Particle
SKU
RC212606L3V
Lenti ORF particles, MNX1 (Myc-DDK-tagged)-Human motor neuron and pancreas homeobox 1 (MNX1), transcript variant 1, 200ul, >10^7 TU/mL
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
---|---|
Tag | Myc-DDK |
Target Symbol | MNX1 |
Synonyms | HB9; HLXB9; HOXHB9; SCRA1 |
Vector | pLenti-C-Myc-DDK-P2A-Puro |
Mammalian Cell Selection | Puromycin |
Sequence Data |
ORF Nucleotide Sequence
The ORF insert of this clone is exactly the same as(RC212606).
|
ACCN | NM_005515 |
ORF Size | 1203 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_005515.3 |
RefSeq Size | 2176 bp |
RefSeq ORF | 1206 bp |
Locus ID | 3110 |
UniProt ID | P50219 |
Cytogenetics | 7q36.3 |
Protein Families | Druggable Genome, ES Cell Differentiation/IPS |
Protein Pathways | Maturity onset diabetes of the young |
MW | 40.57 kDa |
Summary | This gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009] |
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