PTEN Induced Putative Kinase 1 (PINK1) ELISA Kits

PINK1 encodes a serine/threonine protein kinase that localizes to mitochondria. Additionally we are shipping PINK1 Antibodies (258) and PINK1 Proteins (13) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
PINK1 65018 Q9BXM7
PINK1 68943 Q99MQ3
Anti-Rat PINK1 PINK1 298575  
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Catalog No. Reactivity Sensitivity Range Images Quantity Supplier Delivery Price Details
Human < 0.13 ng/mL 0.312 ng/mL - 20 ng/mL   96 Tests Log in to see 11 to 18 Days
  96 Tests Log in to see 15 to 18 Days

More ELISA Kits for PINK1 Interaction Partners

Fruit Fly (Drosophila melanogaster) PTEN Induced Putative Kinase 1 (PINK1) interaction partners

  1. This study found learning and memory abnormalities in PINK1 mutant genotypes in Drosophila.

  2. Drosophila CHIP protects against mitochondrial dysfunction by acting downstream of Pink1 in parallel with Parkin (show PARK2 ELISA Kits)

  3. Maintenance of tissue homeostasis upon reduction of Pink1 or Parkin (show PARK2 ELISA Kits) appears to result from reduction of age- and stress-induced intestinal stem cell proliferation, in part, through induction of ISC senescence.

  4. activation of endoplasmic reticulum stress by defective mitochondria is neurotoxic in pink1 and parkin (show PARK2 ELISA Kits) flies and that the reduction of this signalling is neuroprotective, independently of defective mitochondria.

  5. autophosphorylation of PINK1 is essential for the mitochondrial translocation of Parkin (show PARK2 ELISA Kits) and for subsequent phosphorylation and activation of Parkin (show PARK2 ELISA Kits).

  6. A pink1 genomic knock-in allele was generated to monitor the dynamic expression pattern of PINK1. The spatiotemporal expression pattern of PINK1 correlates with the cell-type specific mitochondrial clearance or persistence. PINK1 and PARKIN (show PARK2 ELISA Kits) function epistatically to mediate timely specific mitophagy during Drosophila midgut metamorphosis.

  7. Our data indicate that PINK1 and Parkin (show PARK2 ELISA Kits) play an important role in FUS (show FUS ELISA Kits)-induced neurodegeneration. This study has uncovered a previously unknown link between FUS (show FUS ELISA Kits) proteinopathy and PINK1/Parkin (show PARK2 ELISA Kits) genes, providing new insights into the pathogenesis of FUS (show FUS ELISA Kits) proteinopathy.

  8. we show that overexpression of Drosophila Clu (show CLU ELISA Kits) complements PINK1, but not parkin (show PARK2 ELISA Kits), mutant muscles. Thus, Clu (show CLU ELISA Kits) is essential for mitochondrial homeostasis and functions in concert with Parkin (show PARK2 ELISA Kits) and VCP (show vcp ELISA Kits) for Marf (show MFN2 ELISA Kits) degradation to promote damaged mitochondrial clearance.

  9. In addition, a PINK1 mutant, which induced mitochondrial enlargement and had been considered as a Drosophila model of Parkinson's disease (PD), caused fly muscle defects, and the loss of vimar could rescue these defects. Furthermore, we found that the mammalian homolog of Vimar, RAP1GDS1, played a similar role in regulating mitochondrial morphology, suggesting a functional conservation of this GEF member.

  10. Buffy has a role enhancing the loss of parkin (show PARK2 ELISA Kits) and suppressing the loss of Pink1 phenotypes in Drosophila

Zebrafish PTEN Induced Putative Kinase 1 (PINK1) interaction partners

  1. Pink1-depleted zebrafish are the first vertebrate model of PINK1 deficiency with loss of dopaminergic neurons.

  2. Our findings suggest that a lack of pink1 in zebrafish alters many vital and critical pathways in addition to the HIF signaling pathway.

  3. Distinct groups of dopaminergic neurons are sensitive to targeted loss of Pink1 factor in a morphant fish model of toxin-induced Parkinson's disease.

  4. Morpholino-mediated loss of pink1 function in zebrafish profoundly affects the development of dopaminergic neurons in the ventral diencephalon and affects behaviour of the zebrafish larvae, namely their response to tactile stimuli and locomotor behavior.

Human PTEN Induced Putative Kinase 1 (PINK1) interaction partners

  1. The results demonstrate that Nix (show BNIP3L ELISA Kits) can serve as an alternative mediator of mitophagy to maintain mitochondrial turnover, identifying Nix (show BNIP3L ELISA Kits) as a promising target for neuroprotective treatment in PINK1/Parkin (show PARK2 ELISA Kits)-related Parkinson's disease.

  2. Studies indicate a functional PTEN-induced putative kinase 1)(PINK1)/E3 ubiquitin protein ligase (parkin (show PARK2 ELISA Kits)) mitophagy pathway in neurons [Review].

  3. PINK1 detection could help stratify patients who may have poor response to chemotherapy and guide the individual treatment.

  4. A mitochondrial protein PINK1 acts as a mitochondrial gatekeeper able to sense the presence of healthy or damaged mitochondria. (Review)

  5. mitochondrial dysfunction activates the PINK1/Parkin (show PARK2 ELISA Kits) signaling and mitophagy in renal tubular epithelial cells under albumin (show ALB ELISA Kits) overload condition.

  6. High Pink1 Expression is Associated with Cancer Progression and Chemo-Resistance in Esophageal Squamous Cell Carcinoma.

  7. Hsp70participated in PINK1-mediated mitophagy by stabilizing PINK1.

  8. This study showed that the heterozygous Pink1 mutation carriers show subtle motor abnormalities when a detailed, specialized motor examination is applied and compared to mutation-negative matched control subjects.

  9. These findings provide evidence for a novel mechanism underlying the protective effects of PINK1 against alpha-syn-induced neurodegeneration and highlight a novel therapeutic target for Parkinson's disease treatment.

  10. Study confirmed that common variants in PARL and PINK1 were associated with leprosy. Furthermore, PARL and PINK1 could physically interact with each other and were involved in the highly connected network formed by reported leprosy susceptibility genes

Mouse (Murine) PTEN Induced Putative Kinase 1 (PINK1) interaction partners

  1. The data supports an indispensable role for Mule in cardiac homeostasis through the regulation of mitochondrial function via maintenance of Pgc-1alpha (show PPARGC1A ELISA Kits) and Pink1 expression and persistent negative regulation of c-Myc (show MYC ELISA Kits).

  2. these data suggest that alleviation of the sustained mitochondrial dysfunction and oxidative stress through co-modulation of NRF2 (show NFE2L2 ELISA Kits) and PINK1 may be in charge of restoration of the cognitive impairments in a mouse model of high-LET carbon ion irradiation

  3. This paper's findings delineate a mechanism by which PINK1 regulates mitochondrial Ca(2 (show CA2 ELISA Kits)+) level through LETM1 and suggest a model by which PINK1 loss leads to deficient phosphorylation of LETM1 and impaired mitochondrial Ca(2 (show CA2 ELISA Kits)+) transport.

  4. PINK1 and PARK2 (show PARK2 ELISA Kits) suppress pancreatic tumorigenesis through control of mitochondrial iron-mediated immunometabolism

  5. This study demonstrated that in the Pink1-/- mouse showed disorder of vocalization and sensorimotor function.

  6. reveal a direct molecular link between nitrosative stress, S-nitrosylated PINK1 formation, and mitophagic dysfunction that contributes to the pathogenesis of Parkinson's disease

  7. In mitochondria from Pink1(-/-) mice, there was a decrease in free chloride and in free supercomplexes in cultured neurons.

  8. These findings provide evidence for a novel mechanism underlying the protective effects of PINK1 against alpha-syn-induced neurodegeneration and highlight a novel therapeutic target for Parkinson's disease treatment.

  9. The results of this study identify PINK1 deficiency as an early modulator of innate immunity in neurons, which precedes late stages of neuroinflammation during alpha-synuclein spreading.

  10. The expression of PINK1 and Parkin (show PARK2 ELISA Kits) were elevated in white adipose tissue in obese mice.

PINK1 Antigen Profile

Antigen 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.

Gene names and symbols associated with PINK1

  • PTEN-induced putative kinase 1 (Pink1) antibody
  • PTEN induced putative kinase 1 (PINK1) antibody
  • PTEN induced putative kinase 1 (pink1) antibody
  • PTEN induced putative kinase 1 (Pink1) antibody
  • 1190006F07Rik antibody
  • AU042772 antibody
  • AW557854 antibody
  • BEST:GH23468 antibody
  • BRPK antibody
  • CG4523 antibody
  • Dmel\\CG4523 antibody
  • dPink1 antibody
  • mFLJ00387 antibody
  • PARK6 antibody
  • PINK antibody
  • pink1 antibody
  • wu:fc39e12 antibody
  • zgc:101729 antibody

Protein level used designations for PINK1

CG4523-PA , CG4523-PB , CG4523-PC , CG4523-PD , CG4523-PE , CG4523-PF , CG4523-PG , CG4523-PH , PTEN induced putative kinase 1 , PTEN-Induced kinase 1 , Pink1-PA , Pink1-PB , Pink1-PC , Pink1-PD , Pink1-PE , Pink1-PF , Pink1-PG , Pink1-PH , PTEN-induced putative kinase 1 , serine/threonine-protein kinase PINK1, mitochondrial , serine/threonine-protein kinase PINK1, mitochondrial-like , PTEN-induced putative kinase protein 1 , protein kinase BRPK

31607 Drosophila melanogaster
425370 Gallus gallus
494085 Danio rerio
510683 Bos taurus
706037 Macaca mulatta
749028 Pan troglodytes
100027082 Monodelphis domestica
100412264 Callithrix jacchus
100443445 Pongo abelii
100465867 Ailuropoda melanoleuca
65018 Homo sapiens
68943 Mus musculus
298575 Rattus norvegicus
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