catalog number :
MBS9429098
products full name :
PINK1 (Phospho-Ser228) Antibody
products short name :
[PINK1]
products name syn :
[BRPK; FLJ27236; mitochondrial; PARK 6; PARK6; Phosphatase and Tensin Homolog; PINK 1; PINK1; PINK1_HUMAN; Protein kinase BRPK; PTEN induced putative kinase 1; PTEN induced putative kinase protein 1; PTEN-induced putative kinase protein 1; Serine/threonine kinase PINK1 mitochondrial; Serine/threonine protein kinase PINK1 mitochondrial; Serine/threonine-protein kinase PINK1;]
other names :
[serine/threonine-protein kinase PINK1, mitochondrial; Serine/threonine-protein kinase PINK1, mitochondrial; serine/threonine-protein kinase PINK1, mitochondrial; PTEN induced putative kinase 1; BRPK; PTEN-induced putative kinase protein 1]
products gene name :
[PINK1]
other gene names :
[PINK1; PINK1; BRPK; PARK6]
reactivity :
Human, Mouse, Rat
specificity :
Phospho-PINK1(Phospho-Ser228) Antibody detects endogenous levels of PINK1 only when phosphorylated at Ser228
purity :
The antibody is from purified rabbit serum by affinity purification via sequential chromatography on phospho- and non-phospho-peptide affinity columns.
form :
In phosphate buffered saline, pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
storage stability :
Store at -20 degree C. Stable for 12 months.
tested application :
Western Blot (WB)
app notes :
WB: 1:500-1:2000
image1 heading :
Western Blot (WB)
other info1 :
Immunogen: A synthesized peptide derived from human PINK1 around the phosphorylation site of Ser228. Immunogen Type: Peptide
products categories :
Phospho-specific Ab
ncbi acc num :
NP_115785.1
ncbi gb acc num :
NM_032409.2
ncbi pathways :
Mitophagy Pathway (1309218); Mitophagy - Animal Pathway (1496831); Mitophagy - Animal Pathway (1496741); Parkinson's Disease Pathway (83098); Parkinsons Disease Pathway (705377); Pink/Parkin Mediated Mitophagy Pathway (1309219)
ncbi summary :
This gene encodes a serine/threonine protein kinase that localizes to mitochondria. It is thought to protect cells from stress-induced mitochondrial dysfunction. Mutations in this gene cause one form of autosomal recessive early-onset Parkinson disease. [provided by RefSeq, Jul 2008]
uniprot summary :
Protects against mitochondrial dysfunction during cellular stress by phosphorylating mitochondrial proteins. Involved in the clearance of damaged mitochondria via selective autophagy (mitophagy) by mediating activation and translocation of PRKN (PubMed:14607334, PubMed:15087508, PubMed:19229105, PubMed:19966284, PubMed:20404107, PubMed:20798600, PubMed:23620051, PubMed:23754282, PubMed:23933751, PubMed:24660806, PubMed:24751536, PubMed:24784582, PubMed:24896179, PubMed:25527291). Targets PRKN to dysfunctional depolarized mitochondria through the phosphorylation of MFN2 (PubMed:23620051). Activates PRKN in 2 steps: (1) by mediating phosphorylation at 'Ser-65' of PRKN and (2) mediating phosphorylation of ubiquitin, converting PRKN to its fully-active form (PubMed:24660806, PubMed:24751536, PubMed:24784582, PubMed:25527291). Required for ubiquinone reduction by mitochondrial complex I by mediating phosphorylation of complex I subunit NDUFA10 ().