Validation Data Gallery
|Positive WB detected in||HeLa cells, HEK-293 cells, PC-12 cells|
|Positive IHC detected in||mouse brain tissue, human brain tissue|
Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0
|Positive IF detected in||mouse brain tissue, rat brain tissue|
|Western Blot (WB)||WB : 1:500-1:1000|
|Immunohistochemistry (IHC)||IHC : 1:1000-1:4000|
|Immunofluorescence (IF)||IF : 1:200-1:800|
|Sample-dependent, check data in validation data gallery|
23274-1-AP targets PINK1 in WB, IHC, IF, CoIP, ELISA applications and shows reactivity with human, mouse, rat samples.
|Tested Reactivity||human, mouse, rat|
|Cited Reactivity||human, mouse, rat, rabbit, zebrafish, pig, duck|
|Host / Isotype||Rabbit / IgG|
|Immunogen||PINK1 fusion protein Ag19825|
|Full Name||PTEN induced putative kinase 1|
|Calculated molecular weight||581 aa, 63 kDa|
|Observed molecular weight||65 kDa, 45 kDa|
|GenBank accession number||BC028215|
|Gene ID (NCBI)||65018|
|Purification Method||Antigen Affinity purified|
|Storage Buffer||PBS with 0.02% sodium azide and 50% glycerol pH 7.3.|
|Storage Conditions||Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. 20ul sizes contain 0.1% BSA.|
PINK1 is a mitochondrial serine/threonine-protein kinase that protects cells from stress-induced mitochondrial dysfunction. The precursor of PINK1 (65 kDa) is synthesized in the cytosol and is imported into the outer membrane of mitochondria. PINK1 is further transferred into the inner membrane. The full-length PINK1 can be proteolytically processed into 52-55 kDa and 45-46 kDa forms (PMID: 18221368; 25108683; 18031932). The half-life of the mature form of PINK1 is very short and it was proposed that the proteasome is involved in its degradation (PMID: 23472196). The gene of PINK1 maps to chromosome 1p36.12. Two alternatively spliced variants exist, the shorter isoform (30 kDa) produced by alternative splicing. Mutations in the PINK1 gene cause autosomal recessive early-onset Parkinson's disease.
Disuse-associated loss of the protease LONP1 in muscle impairs mitochondrial function and causes reduced skeletal muscle mass and strength.
Nucleic Acids Res
DNA damage invokes mitophagy through a pathway involving Spata18.
Deregulated MTOR (mechanistic target of rapamycin kinase) is responsible for autophagy defects exacerbating kidney stone development.
Autophagy regulates functional differentiation of mammary epithelial cells.
CDK9 inhibition blocks the initiation of PINK1-PRKN-mediated mitophagy by regulating the SIRT1-FOXO3-BNIP3 axis and enhances the therapeutic effects involving mitochondrial dysfunction in hepatocellular carcinoma.
Restoration of mitophagy ameliorates cardiomyopathy in Barth syndrome.
The reviews below have been submitted by verified Proteintech customers who received an incentive forproviding their feedback.
Nin (Verified Customer) (02-27-2023)
It is okay to probe PINK1 with two bands although there are some weak non-specific bands.
Yahir Alberto (Verified Customer) (11-12-2021)
The antibody works fine with overnight incubation at 4 °C.
Tanusree (Verified Customer) (12-03-2019)
This antibody works good in western blotting analysis using mouse tissues.
HONGXUE (Verified Customer) (08-19-2019)
The specific is not good. You can detect many bands using WB.