ZBTB20 (NM_001164345) Human Tagged ORF Clone Lentiviral Particle
SKU
RC228990L3V
Lenti ORF particles, ZBTB20 (Myc-DDK-tagged)-Human zinc finger and BTB domain containing 20 (ZBTB20), transcript variant 5, 200ul, >10^7 TU/mL
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
---|---|
Tag | Myc-DDK |
Target Symbol | ZBTB20 |
Synonyms | DPZF; HOF; ODA-8S; PRIMS; ZNF288 |
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(RC228990).
|
ACCN | NM_001164345 |
ORF Size | 2004 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_001164345.1 |
RefSeq Size | 27291 bp |
RefSeq ORF | 2007 bp |
Locus ID | 26137 |
UniProt ID | Q9HC78 |
Cytogenetics | 3q13.31 |
Protein Families | Transcription Factors |
MW | 73.5 kDa |
Summary | This gene, which was initially designated as dendritic cell-derived BTB/POZ zinc finger (DPZF), belongs to a family of transcription factors with an N-terminal BTB/POZ domain and a C-terminal DNA-bindng zinc finger domain. The BTB/POZ domain is a hydrophobic region of approximately 120 aa which mediates association with other BTB/POZ domain-containing proteins. This gene acts as a transcriptional repressor and plays a role in many processes including neurogenesis, glucose homeostasis, and postnatal growth. Mutations in this gene have been associated with Primrose syndrome as well as the 3q13.31 microdeletion syndrome. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Feb 2017] |
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