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Hsp60 (HSPD1) (NM_199440) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC201281L4V
- LentiORF®
-
Lenti ORF particles, HSPD1 (mGFP-tagged) - Human heat shock 60kDa protein 1 (chaperonin) (HSPD1), nuclear gene encoding mitochondrial protein, transcript variant 2, 200ul, >10^7 TU/mL
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CNY 11,590.00
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CNY 2,700.00
Specifications
| Product Data | |
| Product Name | Hsp60 (HSPD1) (NM_199440) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | CPN60; GROEL; HLD4; HSP-60; HSP60; HSP65; HuCHA60; SPG13 |
| Vector | pLenti-C-mGFP-P2A-Puro |
| ACCN | NM_199440 |
| ORF Size | 1719 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC201281).
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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_199440.1, NP_955472.1 |
| RefSeq Size | 2319 bp |
| RefSeq ORF | 1722 bp |
| Locus ID | 3329 |
| Protein Families | Druggable Genome, Stem cell - Pluripotency |
| Protein Pathways | RNA degradation, Type I diabetes mellitus |
| MW | 61.1 kDa |
| Gene Summary | This gene encodes a member of the chaperonin family. The encoded mitochondrial protein may function as a signaling molecule in the innate immune system. This protein is essential for the folding and assembly of newly imported proteins in the mitochondria. This gene is adjacent to a related family member and the region between the 2 genes functions as a bidirectional promoter. Several pseudogenes have been associated with this gene. Two transcript variants encoding the same protein have been identified for this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 13. [provided by RefSeq, Jun 2010] |
Documents
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