SHFM1 (SEM1) (NM_006304) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC207564L4V
- LentiORF®
Lenti ORF particles, SHFM1 (mGFP-tagged) - Human split hand/foot malformation (ectrodactyly) type 1 (SHFM1), 200ul, >10^7 TU/mL
Lentiviral Particles: DDK DDK w/ Puro mGFP
AAV Particle: DDK
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Specifications
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
Tag | mGFP |
Symbol | SEM1 |
Synonyms | C7orf76; DSS1; ECD; PSMD15; SHFD1; Shfdg1; SHFM1; SHSF1 |
Mammalian Cell Selection | Puromycin |
Vector | pLenti-C-mGFP-P2A-Puro |
ACCN | NM_006304 |
ORF Size | 210 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC207564).
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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_006304.1, NP_006295.1 |
RefSeq Size | 509 bp |
RefSeq ORF | 213 bp |
Locus ID | 7979 |
UniProt ID | P60896 |
Cytogenetics | 7q21.3 |
Domains | DSS1_SEM1 |
Protein Pathways | Homologous recombination, Proteasome |
MW | 8.3 kDa |
Gene Summary | The product of this gene has been localized within the split hand/split foot malformation locus SHFM1 at chromosome 7. It has been proposed to be a candidate gene for the autosomal dominant form of the heterogeneous limb developmental disorder split hand/split foot malformation type 1. In addition, it has been shown to directly interact with BRCA2. It also may play a role in the completion of the cell cycle. [provided by RefSeq, Jul 2008] |
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