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PARL encodes a mitochondrial integral membrane protein. Additionally we are shipping PARL Proteins (4) and many more products for this protein.
Showing 10 out of 46 products:
Human Monoclonal PARL Primary Antibody for ELISA, WB - ABIN969340
Strausberg, Feingold, Grouse, Derge, Klausner, Collins, Wagner, Shenmen, Schuler, Altschul, Zeeberg, Buetow, Schaefer, Bhat, Hopkins, Jordan, Moore, Max, Wang, Hsieh, Diatchenko, Marusina, Farmer et al.: Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. ... in Proceedings of the National Academy of Sciences of the United States of America 2002
Show all 3 Pubmed References
Chicken Polyclonal PARL Primary Antibody for ELISA, ICC - ABIN4343719
Jeyaraju, Xu, Letellier, Bandaru, Zunino, Berg, McBride, Pellegrini: Phosphorylation and cleavage of presenilin-associated rhomboid-like protein (PARL) promotes changes in mitochondrial morphology. in Proceedings of the National Academy of Sciences of the United States of America 2006
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Cow (Bovine) Polyclonal PARL Primary Antibody for IHC, WB - ABIN2782038
Walder, Kerr-Bayles, Civitarese, Jowett, Curran, Elliott, Trevaskis, Bishara, Zimmet, Mandarino, Ravussin, Blangero, Kissebah, Collier: The mitochondrial rhomboid protease PSARL is a new candidate gene for type 2 diabetes. in Diabetologia 2005
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Human Monoclonal PARL Primary Antibody for ELISA, WB - ABIN966805
McQuibban, Saurya, Freeman: Mitochondrial membrane remodelling regulated by a conserved rhomboid protease. in Nature 2003
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PARL preserves mitochondrial membrane homeostasis via STARD7 (show STARD7 Antibodies) processing and is emerging as a critical regulator of protein localization between mitochondria and the cytosol
Study confirmed that common variants in PARL and PINK1 (show PINK1 Antibodies) were associated with leprosy. Furthermore, PARL and PINK1 (show PINK1 Antibodies) could physically interact with each other and were involved in the highly connected network formed by reported leprosy susceptibility genes.
PDK2 (show PDK2 Antibodies)/PARL senses defects in mitochondrial bioenergetics.
Adipogenic process can be dissected into 3 stages according to the participation of PARL-PINK1 (show PINK1 Antibodies)-Parkin (show PARK2 Antibodies) system. Findings reveal the sequential adipogenic events directed by PARL-PINK1 (show PINK1 Antibodies)-Parkin (show PARK2 Antibodies) system, add more evidence supporting the convergence of pathogenesis leading to neurodegenerative and metabolic disease
These findings enrich the allelic spectrum of ABCC5 (show ABCC5 Antibodies) in PACG. We identified no tagging SNP responsible for the association of the whole region.
These results reveal a pro-apoptotic function of PARL and identify PARL-mediated Smac (show DIABLO Antibodies) processing and cytochrome c (show CYCS Antibodies) release facilitated by OPA1 (show OPA1 Antibodies)-dependent cristae remodelling as two independent pro-apoptotic pathways in mitochondria.
pathogenic PINK1 (show PINK1 Antibodies) mutants which are not cleaved by PARL affect PINK1 (show PINK1 Antibodies) kinase activity and the ability to induce PARK2 (show PARK2 Antibodies)-mediated mitophagy.
Common genetic variants of the PINK1 (show PINK1 Antibodies) and PARL genes are unlikely to be involved in schizophrenia.
the frequency of the haplotype AAC, and AAT were significantly higher in the unaffected cases and the frequencies of haplotype GGT were significantly higher in LHON cases
Rhomboid protease PARL mediates the mitochondrial membrane potential loss-induced cleavage of PGAM5 (show PGAM5 Antibodies).
Downregulation of PARL after ischemia is a key step in ischemic neuronal injury, and that it decreases HtrA2 (show HTRA2 Antibodies) processing and increases neuronal vulnerability.
the OPA1 (show MED12 Antibodies)/PARL dependent pathway of cristae remodeling is implicated in heat shock.
Suppression of PARL protein in healthy myotubes lowered mitochondrial mass and insulin (show INS Antibodies)-stimulated glycogen (show GYS1 Antibodies) synthesis and increased reactive oxygen species production.
results indicate a different function and mechanism of Hax1 (show HAX1 Antibodies) in apoptosis and re-opens the question of whether mammalian PARL, in addition to apoptosis, regulates mitochondrial stress response through Omi/HtrA2 (show HTRA2 Antibodies) processing.
Parl-/- mitochondria display reduced levels of OPA1 (show MED12 Antibodies), and OPA1 (show MED12 Antibodies) specifically targeted to IMS complements Parl-/- cells, substantiating the importance of PARL in OPA1 (show MED12 Antibodies) processing.(PARL protein, mouse)
Hax1 (show HAX1 Antibodies), is required to suppress apoptosis in lymphocytes and neurons; suppression requires the interaction of Hax1 (show HAX1 Antibodies) with the mitochondrial proteases Parl and HtrA2 (show HTRA2 Antibodies)
This gene encodes a mitochondrial integral membrane protein. Following proteolytic processing of this protein, a small peptide (P-beta) is formed and translocated to the nucleus. This gene may be involved in signal transduction via regulated intramembrane proteolysis of membrane-tethered precursor proteins. Variation in this gene has been associated with increased risk for type 2 diabetes. Alternative splicing results in multiple transcript variants encoding different isoforms.
mitochondrial intramembrane cleaving protease PARL
, mitochondrial intramembrane-cleaving protease PARL
, presenilins-associated rhomboid-like protein, mitochondrial
, rhomboid 7 homolog 1
, presenilin associated, rhomboid-like isoform 1 preproprotein
, presenilin associated, rhomboid-like preproprotein