United States
Germany
Japan
United Kingdom
China
HOXD9 (NM_014213) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC206492L4V
- LentiORF®
-
Lenti ORF particles, HOXD9 (mGFP-tagged)-Human homeobox D9 (HOXD9), 200ul, >10^7 TU/mL
Need custom lentivirus service?
Get a free quote
CNY 9,975.00
货期*
详询
规格
Product images
经常一起买 (3)
HOXD9 mouse monoclonal antibody,clone OTI1H3
CNY 1,999.00
CNY 2,700.00
Specifications
| Product Data | |
| Product Name | HOXD9 (NM_014213) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | Hox-4.3; Hox-5.2; HOX4; HOX4C |
| Vector | pLenti-C-mGFP-P2A-Puro |
| ACCN | NM_014213 |
| ORF Size | 1026 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC206492).
|
| 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_014213.2 |
| RefSeq Size | 1902 bp |
| RefSeq ORF | 1059 bp |
| Locus ID | 3235 |
| Protein Families | Transcription Factors |
| MW | 35.6 kDa |
| Gene Summary | This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXD genes located at 2q31-2q37 chromosome regions. Deletions that removed the entire HOXD gene cluster or 5' end of this cluster have been associated with severe limb and genital abnormalities. The exact role of this gene has not been determined. [provided by RefSeq, Jul 2008] |
Documents
| Product Manuals |
| FAQs |
| SDS |
Resources
You may also need
Customer
Reviews
Loading...
