HSP27 (HSPB1) (NM_001540) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC201800L2V
- LentiORF®
Lenti ORF particles, HSPB1 (mGFP-tagged) - Human heat shock 27kDa protein 1 (HSPB1), 200ul, >10^7 TU/mL
Lentiviral Particles: DDK DDK w/ Puro mGFP w/ Puro
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USD 365.00
Specifications
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
Tag | mGFP |
Symbol | HSP27 |
Synonyms | CMT2F; HEL-S-102; HMN2B; HS.76067; Hsp25; HSP27; HSP28; SRP27 |
Mammalian Cell Selection | None |
Vector | pLenti-C-mGFP |
ACCN | NM_001540 |
ORF Size | 615 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC201800).
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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_001540.2 |
RefSeq Size | 914 bp |
RefSeq ORF | 618 bp |
Locus ID | 3315 |
UniProt ID | P04792 |
Cytogenetics | 7q11.23 |
Domains | HSP20 |
Protein Pathways | MAPK signaling pathway, VEGF signaling pathway |
MW | 22.8 kDa |
Gene Summary | This gene encodes a member of the small heat shock protein (HSP20) family of proteins. In response to environmental stress, the encoded protein translocates from the cytoplasm to the nucleus and functions as a molecular chaperone that promotes the correct folding of other proteins. This protein plays an important role in the differentiation of a wide variety of cell types. Expression of this gene is correlated with poor clinical outcome in multiple human cancers, and the encoded protein may promote cancer cell proliferation and metastasis, while protecting cancer cells from apoptosis. Mutations in this gene have been identified in human patients with Charcot-Marie-Tooth disease and distal hereditary motor neuropathy. [provided by RefSeq, Aug 2017] |
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