HOXD8 (NM_019558) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC205062L3V
- LentiORF®
Lenti ORF particles, HOXD8 (Myc-DDK tagged) - Human homeobox D8 (HOXD8), transcript variant 1, 200ul, >10^7 TU/mL
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Specifications
Product Data | |
Product Name | HOXD8 (NM_019558) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | HOX4; HOX4E; HOX5.4 |
Vector | pLenti-C-Myc-DDK-P2A-Puro |
ACCN | NM_019558 |
ORF Size | 597 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC205062).
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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_019558.2 |
RefSeq Size | 2599 bp |
RefSeq ORF | 873 bp |
Locus ID | 3234 |
Domains | homeobox |
Protein Families | ES Cell Differentiation/IPS, Transcription Factors |
MW | 31.8 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 in a cluster on chromosome 2. Deletions that remove the entire HOXD gene cluster or the 5' end of this cluster have been associated with severe limb and genital abnormalities. In addition to effects during embryogenesis, this particular gene may also play a role in adult urogenital tract function. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Dec 2010] |
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