WDR9 (BRWD1) (NM_001007246) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC217768L4V
- LentiORF®
-
Lenti ORF particles, BRWD1 (mGFP-tagged)-Human bromodomain and WD repeat domain containing 1 (BRWD1), transcript variant 3, 200ul, >10^7 TU/mL
Lentiviral Particles: DDK w/ Puro
Product Images
![](https://cdn.origene.com/img/defaults-img.jpg)
Frequently bought together (3)
Other products for "WDR9"
Specifications
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
Tag | mGFP |
Symbol | WDR9 |
Synonyms | C21orf107; DCAF19; N143; WDR9; WRD9 |
Mammalian Cell Selection | Puromycin |
Vector | pLenti-C-mGFP-P2A-Puro |
ACCN | NM_001007246 |
ORF Size | 360 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC217768).
|
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_001007246.2, NP_001007247.1 |
RefSeq Size | 2653 bp |
RefSeq ORF | 363 bp |
Locus ID | 54014 |
UniProt ID | Q9NSI6 |
Cytogenetics | 21q22.2 |
MW | 13.6 kDa |
Gene Summary | This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD) residues which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes including cell cycle progression, signal transduction, apoptosis, and gene regulation. This protein contains 2 bromodomains and multiple WD repeats. This gene is located within the Down syndrome region-2 on chromosome 21. Alternative splicing of this gene generates multiple transcript variants encoding distinct isoforms. In mouse, this gene encodes a nuclear protein that has a polyglutamine-containing region that functions as a transcriptional activation domain which may regulate chromatin remodelling and associates with a component of the SWI/SNF chromatin remodelling complex.[provided by RefSeq, Jun 2011] |
Documents
Product Manuals |
FAQs |
SDS |
Resources
{0} Product Review(s)
0 Product Review(s)
Submit review
Be the first one to submit a review
Product Citations
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen
complexities in the preparation of your product. International customers may expect an additional 1-2 weeks
in shipping.