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FAM134B (RETREG1) (NM_001034850) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC208619L4V
- LentiORF®
-
Lenti ORF particles, FAM134B (mGFP-tagged) - Human family with sequence similarity 134, member B (FAM134B), transcript variant 1, 200ul, >10^7 TU/mL
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CNY 9,975.00
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规格
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Specifications
| Product Data | |
| Product Name | FAM134B (RETREG1) (NM_001034850) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | FAM134B; JK-1; JK1 |
| Vector | pLenti-C-mGFP-P2A-Puro |
| ACCN | NM_001034850 |
| ORF Size | 1491 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC208619).
|
| OTI Disclaimer | Due to the inherent nature of this plasmid, standard methods to replicate additional amounts of DNA in E. coli are highly likely to result in mutations and/or rearrangements. Therefore, OriGene does not guarantee the capability to replicate this plasmid DNA. Additional amounts of DNA can be purchased from OriGene with batch-specific, full-sequence verification at a reduced cost. Please contact our customer care team at custsupport@origene.com or by calling 301.340.3188 option 3 for pricing and delivery. 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_001034850.1, NP_001030022.1 |
| RefSeq Size | 3308 bp |
| RefSeq ORF | 1494 bp |
| Locus ID | 54463 |
| Protein Families | Transmembrane |
| MW | 54.7 kDa |
| Gene Summary | The protein encoded by this gene is a cis-Golgi transmembrane protein that may be necessary for the long-term survival of nociceptive and autonomic ganglion neurons. Mutations in this gene are a cause of hereditary sensory and autonomic neuropathy type IIB (HSAN IIB), and this gene may also play a role in susceptibility to vascular dementia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011] |
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