SIX1 (NM_005982) Human Tagged ORF Clone Lentiviral Particle
SKU
RC203465L3V
Lenti ORF particles, SIX1 (Myc-DDK tagged) - Human SIX homeobox 1 (SIX1), 200ul, >10^7 TU/mL
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
---|---|
Tag | Myc-DDK |
Target Symbol | SIX1 |
Synonyms | BOS3; DFNA23; TIP39 |
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(RC203465).
|
ACCN | NM_005982 |
ORF Size | 852 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_005982.1 |
RefSeq Size | 2687 bp |
RefSeq ORF | 855 bp |
Locus ID | 6495 |
UniProt ID | Q15475 |
Cytogenetics | 14q23.1 |
Protein Families | Transcription Factors |
MW | 32.2 kDa |
Summary | The protein encoded by this gene is a homeobox protein that is similar to the Drosophila 'sine oculis' gene product. This gene is found in a cluster of related genes on chromosome 14 and is thought to be involved in limb development. Defects in this gene are a cause of autosomal dominant deafness type 23 (DFNA23) and branchiootic syndrome type 3 (BOS3). [provided by RefSeq, Jul 2008] |
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