C1orf124 (SPRTN) (NM_001010984) Human Tagged ORF Clone
CAT#: RG218238
- TrueORF®
SPRTN (GFP-tagged) - Human chromosome 1 open reading frame 124 (C1orf124), transcript variant 2
"NM_001010984" in other vectors (4)
Product Images
![](https://cdn.origene.com/img/defaults-img-expression-plasmids.jpg)
Specifications
Product Data | |
Type | Human Tagged ORF Clone |
Tag | TurboGFP |
Symbol | SPRTN |
Synonyms | C1orf124; DVC1; PRO4323; spartan |
Vector | pCMV6-AC-GFP |
E. coli Selection | Ampicillin (100 ug/mL) |
Mammalian Cell Selection | Neomycin |
Sequence Data |
>RG218238 representing NM_001010984
Red=Cloning site Blue=ORF Green=Tags(s) TTTTGTAATACGACTCACTATAGGGCGGCCGGGAATTCGTCGACTGGATCCGGTACCGAGGAGATCTGCC GCCGCGATCGCC ATGGATGATGACTTGATGTTGGCACTGCGGCTTCAGGAGGAGTGGAACTTGCAGGAGGCGGAGCGCGATC ATGCCCAGGAGTCCCTGTCGCTAGTGG ACGCGTACGCGGCCGCTCGAG - GFP Tag - GTTTAA >RG218238 representing NM_001010984
Red=Cloning site Green=Tags(s) MDDDLMLALRLQEEWNLQEAERDHAQESLSLV TRTRRLE - GFP Tag - V |
Restriction Sites |
SgfI-MluI
Cloning Scheme for this gene
Plasmid Map
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ACCN | NM_001010984 |
ORF Size | 750 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. |
Reference Data | |
RefSeq | NM_001010984.1, NP_001010984.1 |
RefSeq Size | 3854 |
RefSeq ORF | 753 |
Locus ID | 83932 |
Protein Families | Druggable Genome |
Gene Summary | The protein encoded by this gene may play a role in DNA repair during replication of damaged DNA. This protein recruits valosin containing protein (p97) to stalled DNA replication forks where it may prevent excessive translesional DNA synthesis and limit the number of DNA-damage induced mutations. It may also be involved in replication-related G2/M-checkpoint regulation. Deficiency of a similar protein in mouse causes chromosomal instability and progeroid phenotypes. Mutations in this gene have been associated with Ruijs-Aalfs syndrome (RJALS). Alternatively spliced transcript variants have been identified. [provided by RefSeq, Mar 2015] |
Documents
Product Manuals |
FAQs |
SDS |
Resources
Other Versions
SKU | Description | Size | Price |
---|---|---|---|
SC301558 | SPRTN (untagged)-Human chromosome 1 open reading frame 124 (C1orf124), transcript variant 2 |
USD 420.00 |
|
RC218238 | SPRTN (Myc-DDK-tagged)-Human chromosome 1 open reading frame 124 (C1orf124), transcript variant 2 |
USD 420.00 |
|
RC218238L3 | Lenti ORF clone of Human chromosome 1 open reading frame 124 (C1orf124), transcript variant 2, Myc-DDK-tagged |
USD 620.00 |
|
RC218238L4 | Lenti ORF clone of Human chromosome 1 open reading frame 124 (C1orf124), transcript variant 2, mGFP tagged |
USD 620.00 |
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