PELO Positive Control for STJ502413 peptide (STJ504686)

SPECIFICATIONS
STJ504686-5
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General Information

Short DescriptionPELO Positive Control for STJ502413 is synthetically produced from the sequence and is suitable for use in western blot applications.
ApplicationsWB
NoteSTRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT TO BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.

Product Properties

Dilution RangeWB: 1:500
FormulationProvided as 100 uL ready-to-use, in SDS-PAGE sample buffer (Laemelli's buffer) containing Tris, pH 6.8, 1 % SDS, Glycerol and Bromophenolblue blue as tracking dye. The sample is reduced by adding 2% beta mercaptoethanol. The protein concentration is
Storage InstructionStore at-20°C for long term storage. Avoid freeze-thaw cycles.

Target Information

Gene SymbolPELO
Gene ID53918
Uniprot IDPELO_HUMAN
SpecificityThis is positive control is recommended for use in combination with PELO antibody STJ502413.

Additional Info

Tissue Specificity Ubiquitously expressed.
Function Component of the Pelota-HBS1L complex, a complex that recognizes stalled ribosomes and triggers the No-Go Decay (NGD) pathway. In the Pelota-HBS1L complex, PELO recognizes ribosomes stalled at the 3' end of an mRNA and engages stalled ribosomes by destabilizing mRNA in the mRNA channel. Following mRNA extraction from stalled ribosomes by the SKI complex, the Pelota-HBS1L complex promotes recruitment of ABCE1, which drives the disassembly of stalled ribosomes, followed by degradation of damaged mRNAs as part of the NGD pathway. As part of the PINK1-regulated signaling, upon mitochondrial damage is recruited to the ribosome/mRNA-ribonucleoprotein complex associated to mitochondrial outer membrane thereby enabling the recruitment of autophagy receptors and induction of mitophagy.
Peptide Name Protein Pelota Homolog
Hpelota
Protein Dom34 Homolog
Cellular Localisation Cytoplasm
Alternative Peptide Names Protein Pelota Homolog protein
Hpelota protein
Protein Dom34 Homolog protein
PELO protein
CGI-17 protein

Information sourced from Uniprot.org

Citations

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