C19orf12 (NM_001031726) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC216851L1V
- LentiORF®
-
Lenti ORF particles, C19orf12 (Myc-DDK tagged) - Human chromosome 19 open reading frame 12 (C19orf12), transcript variant 1, 200ul, >10^7 TU/mL
Need custom lentivirus service?
Get a free quote
CNY 7,410.00
货期*
详询
规格
Cited in 1 publication. |
Product images
![](https://cdn.origene.com/img/defaults-img.jpg)
经常一起买 (2)
Specifications
Product Data | |
Product Name | C19orf12 (NM_001031726) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | MPAN; NBIA3; NBIA4; SPG43 |
Vector | pLenti-C-Myc-DDK |
ACCN | NM_001031726 |
ORF Size | 456 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC216851).
|
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_001031726.2, NP_001026896.2 |
RefSeq Size | 4431 bp |
RefSeq ORF | 459 bp |
Locus ID | 83636 |
Protein Families | Transmembrane |
MW | 16.1 kDa |
Gene Summary | This gene encodes a small transmembrane protein. Mutations in this gene are a cause of neurodegeneration with brain iron accumulation-4 (NBIA4), but the specific function of the encoded protein is unknown. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011] |
Citations (1)
The use of this cDNA Clones has been cited in the following citations: |
---|
Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation
,null,
American Journal of Human Genetics
,PubMed ID 21981780
[C19orf12]
|
Documents
Product Manuals |
FAQs |
SDS |
Resources
You may also need
其它C19orf12产品
Customer
Reviews
Loading...