AIPL1 (NM_001033054) Human Tagged ORF Clone
CAT#: RC218193L3
- LentiORF®
Lenti-ORF clone of AIPL1 (Myc-DDK-tagged)-Human aryl hydrocarbon receptor interacting protein-like 1 (AIPL1), transcript variant 2
"NM_001033054" in other vectors (4)
Product Images
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Specifications
Product Data | |
Type | Human Tagged ORF Clone |
Tag | Myc-DDK |
Symbol | AIPL1 |
Synonyms | AIPL2; LCA4 |
Vector | pLenti-C-Myc-DDK-P2A-Puro |
E. coli Selection | Chloramphenicol (34 ug/mL) |
Mammalian Cell Selection | Puromycin |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC218193).
|
Restriction Sites | SgfI-MluI Cloning Scheme for this gene |
ACCN | NM_001033054 |
ORF Size | 963 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_001033054.1, NP_001028226.1 |
RefSeq Size | 2792 |
RefSeq ORF | 966 |
Locus ID | 23746 |
Protein Families | Druggable Genome |
MW | 36.5 kDa |
Gene Summary | Leber congenital amaurosis (LCA) is the most severe inherited retinopathy with the earliest age of onset and accounts for at least 5% of all inherited retinal diseases. Affected individuals are diagnosed at birth or in the first few months of life with nystagmus, severely impaired vision or blindness and an abnormal or flat electroretinogram. The photoreceptor/pineal-expressed gene, AIPL1, encoding aryl-hydrocarbon interacting protein-like 1, is located within the LCA4 candidate region. The encoded protein contains three tetratricopeptide motifs, consistent with chaperone or nuclear transport activity. Mutations in this gene may cause approximately 20% of recessive LCA. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014] |
Documents
Product Manuals |
FAQs |
SDS |
Resources
Other Versions
SKU | Description | Size | Price |
---|---|---|---|
SC302689 | AIPL1 (untagged)-Human aryl hydrocarbon receptor interacting protein-like 1 (AIPL1), transcript variant 2 |
USD 660.00 |
|
RC218193 | AIPL1 (Myc-DDK-tagged)-Human aryl hydrocarbon receptor interacting protein-like 1 (AIPL1), transcript variant 2 |
USD 420.00 |
|
RG218193 | AIPL1 (GFP-tagged) - Human aryl hydrocarbon receptor interacting protein-like 1 (AIPL1), transcript variant 2 |
USD 460.00 |
|
RC218193L4 | Lenti-ORF clone of AIPL1 (mGFP-tagged)-Human aryl hydrocarbon receptor interacting protein-like 1 (AIPL1), transcript variant 2 |
USD 620.00 |
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