anti-Palmitoyl-Protein Thioesterase 1 (PPT1) Antibodies

The protein encoded by PPT1 is a small glycoprotein involved in the catabolism of lipid-modified proteins during lysosomal degradation. Additionally we are shipping PPT1 Proteins (13) and PPT1 Kits (7) and many more products for this protein.

list all antibodies Gene Name GeneID UniProt
PPT1 5538 P50897
PPT1 19063 O88531
PPT1 29411 P45479
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Top anti-PPT1 Antibodies at antibodies-online.com

Showing 10 out of 107 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Delivery Price Details
Human Rabbit Un-conjugated IHC (p), WB IHC(P): Human Intestinal Cancer Tissue 100 μg 4 to 6 Days
$280.00
Details
Cow Rabbit Un-conjugated WB 100 μL 2 to 3 Days
$289.00
Details
Human Mouse Un-conjugated IHC, IHC (p), WB 100 μL 11 to 14 Days
$522.50
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Human Rabbit Un-conjugated EIA, IHC (p), WB 0.4 mL 6 to 8 Days
$484.00
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Human Rabbit Un-conjugated EIA, IHC (p), WB 0.4 mL 6 to 8 Days
$484.00
Details
Human Mouse Un-conjugated WB All lanes : Anti-PPT1 Antibody (C-term) at 1:2000 dilution Lane 1: Hela whole cell lysates Lane 2: HepG2 whole cell lysates Lysates/proteins at 20 μg per lane. Secondary Goat Anti-mouse IgG, (H+L), Peroxidase conjugated at 1/10000 dilution Predicted band size : 34 kDa Blocking/Dilution buffer: 5% NFDM/TBST. Dilution: 1:2000 400 μL 10 to 11 Days
$385.00
Details
Human Mouse Un-conjugated FACS, IHC (p), WB   100 μg 4 to 6 Days
$280.00
Details
Human Rabbit Un-conjugated WB Western blot analysis of hPPT1-C46 (ABIN389116) in mouse cerebellum tissue lysates (35 µg/lane).PPT1 (arrow) was detected using the purified polyclonal antibody. 400 μL 10 to 11 Days
$385.00
Details
Human Rabbit Un-conjugated IHC (p), WB Western blot analysis of PPT1 Antibody (C-term) (ABIN389117) in 293 cell line lysates (35 µg/lane). PPT1 (arrow) was detected using the purified polyclonal antibody. Formalin-fixed and paraffin-embedded human lung carcinoma tissue reacted with PPT1 antibody (C-term) (ABIN389117), which was peroxidase-conjugated to the secondary antibody, followed by DAB staining. 400 μL 10 to 11 Days
$385.00
Details
Human Rabbit Un-conjugated ELISA, WB Western blot analysis of PPT1 using Jurkat whole  lysates. 100 μL 11 to 12 Days
$390.77
Details

Top referenced anti-PPT1 Antibodies

  1. Human Monoclonal PPT1 Primary Antibody for WB - ABIN1944801 : Crews, Lane, Schreiber: Didemnin binds to the protein palmitoyl thioesterase responsible for infantile neuronal ceroid lipofuscinosis. in Proceedings of the National Academy of Sciences of the United States of America 1996 (PubMed)
    Show all 4 Pubmed References

  2. Human Polyclonal PPT1 Primary Antibody for IHC (p), ELISA - ABIN543470 : Calero, Gupta, Nonato, Tandel, Biehl, Hofmann, Clardy: The crystal structure of palmitoyl protein thioesterase-2 (PPT2) reveals the basis for divergent substrate specificities of the two lysosomal thioesterases, PPT1 and PPT2. in The Journal of biological chemistry 2003 (PubMed)
    Show all 3 Pubmed References

  3. Human Polyclonal PPT1 Primary Antibody for IHC (p), ELISA - ABIN543469 : Weimer, Kriscenski-Perry, Elshatory, Pearce: The neuronal ceroid lipofuscinoses: mutations in different proteins result in similar disease. in Neuromolecular medicine 2002 (PubMed)
    Show all 3 Pubmed References

  4. Dog (Canine) Monoclonal PPT1 Primary Antibody for WB - ABIN2729521 : Segal-Salto, Sapir, Reiner: Reversible Cysteine Acylation Regulates the Activity of Human Palmitoyl-Protein Thioesterase 1 (PPT1). in PLoS ONE 2016 (PubMed)

  5. Human Polyclonal PPT1 Primary Antibody for IHC, IHC (p) - ABIN4347151 : Scifo, Szwajda, Soliymani, Pezzini, Bianchi, Dapkunas, Dębski, Uusi-Rauva, Dadlez, Gingras, Tyynelä, Simonati, Jalanko, Baumann, Lalowski: Quantitative analysis of PPT1 interactome in human neuroblastoma cells. in Data in brief 2015 (PubMed)

More Antibodies against PPT1 Interaction Partners

Human Palmitoyl-Protein Thioesterase 1 (PPT1) interaction partners

  1. The results demonstrate that these patient iPSC derived NCL NSCs are valid cell- based disease models with characteristic disease phenotypes that can be used for study of disease pathophysiology and drug development.

  2. the study contributes four novel variants to the spectrum of PPT1 gene mutations and eight novel variants to the TPP1 gene mutation data in neuronal ceroid lipofuscinoses type I and type II

  3. Targeting PPT1 blocks mTOR signaling in a manner distinct from catalytic inhibitors, while concurrently inhibiting autophagy, thereby providing a new strategy for cancer therapy.

  4. the combination of elevated glycolysis and deficient MRPL13 activity was closely linked to CLN1-mediated tumor activity in human hepatoma cells

  5. Proteomics analysis on isolated cilia revealed 660 proteins, which differed in their abundance levels between wild type and Ppt1 knock out.

  6. we reveal the existence of a positive feedback loop, where palmitoylation of PPT1 results in decreased activity and subsequent elevation in the amount of palmitoylated proteins.

  7. analysis of the palmitoyl protein thioesterase 1 interactome in SH-SY5Y human neuroblastoma cells

  8. Data (including data from knockout mice) suggest that deficiency of PPT1 leads to accumulation of granular osmiophilic deposits in many cell types, especially in astrocytes. [review-like article]

  9. Data suggest that human monocytes and macrophages express PPT1; PPT1 appears to contribute 32-40% of 2-arachidonylglycerol hydrolysis activity in THP1 monocyte cell line.

  10. This neuroimaging finding in PPT1-related neuronal ceroid lipofuscinosis was not previously reported.

  11. Stop codon read-through with PTC124 induces palmitoyl-protein thioesterase-1 activity, reduces thioester load and suppresses apoptosis in cultured cells from Infantile neuronal ceroid lipofuscinosis patients.

  12. Results describe the correlation between the three-dimensional structural changes in mutant palmitoyl protein thioesterase 1 and biochemical phenotypes.

  13. mutated in neuronal ceroid lipofuscinosis

  14. The clinical, biochemical, and molecular genetic aspects of lysosomal storage disorders are discussed in this review

  15. The crystal structure of palmitoyl protein thioesterase-2 (PPT2) reveals the basis for divergent substrate specificities of the two lysosomal thioesterases, PPT1 and PPT2.

  16. there is a close correlation between CLN2 and CLN1 expression and colorectal carcinoma progression and metastasis and suggest that they may be potential molecular targets

  17. Results show that PPT1-deficiency causes a defect in fluid-phase and receptor-mediated endocytosis.

  18. ER stress due to PPT1-deficiency increases ROS and disrupts calcium homeostasis activating caspase-9 and caspase-9 activation mediates caspase-3 activation and apoptosis contributing to rapid neurodegeneration in INCL.

  19. Adult neuronal ceroid lipofuscinosis caused by deficiency in palmitoyl protein thioesterase 1.

  20. Palmitoyl protein thioesterase-1 deficiency impairs synaptic vesicle recycling at nerve terminals in humans and mice

Mouse (Murine) Palmitoyl-Protein Thioesterase 1 (PPT1) interaction partners

  1. Thes findings of this stuidy suggest that both Ppt1(-/-) microglia and astrocytes are dysfunctional and may contribute to the neurodegeneration observed in infantile neuronal ceroid lipofuscinosis disease

  2. Our results indicate that PPT1 deficiency causes alterations in the mitochondrial respiratory chain.

  3. Proteomics analysis on isolated cilia revealed 660 proteins, which differed in their abundance levels between wild type and Ppt1 knock out.

  4. In the novel Cln1(R151X) mouse model of INCL.

  5. Parkinson-like motor/sensorimotor deficits in Cln1-/- mice are not mediated by dopamine deficiency.

  6. Data show that Cln1 mutations disrupt the maturation of cathepsin D in lysosome contributing to neuropathology of infantile neuronal ceroid lipofuscinoses and suggest cathepsin D deficiency to be common link between infantile and congenital form.

  7. The authors have generated a Cln1 R151X point mutation mouse model that recapitulates the molecular, neuropathological and behavioral phenotypes of neuronal ceroid lipofuscinoses.

  8. Data (including data from knockout mice) suggest that deficiency of Ppt1 leads to accumulation of granular osmiophilic deposits in many cell types, especially in astrocytes. [review-like article]

  9. Data suggest that mouse macrophages express PPT1; PPT1 appears to contribute to 2-arachidonylglycerol hydrolysis activity in peritoneal macrophages in culture.

  10. The simultaneous loss of both Cln1 and Cln5 genes might enhance the typical pathological phenotypes of these mice by disrupting or downregulating shared or convergent pathogenic pathways.

  11. These results uncover a previously unknown phenotype associated with PPT1 deficiency, that of altered thermoregulation, which is associated with impaired lipolysis and neurotransmitter release to brown adipose tissue during cold exposure.

  12. The addition of the small molecule PPT1 mimetic can further increase that response.

  13. Glutamate receptor 4 (GluR4) AMPA receptor hypofunction and NMDA receptor hyperfunction phenotype show increased sensitivity in Ppt1-deficient neurons.

  14. Data show a progressive breakdown of axons and synapses in the brains of two different models of NCL: Ppt1(-/-) model of infantile NCL and Cln6(nclf) model of variant late-infantile NCL.

  15. The polarized axonal targeting of PPT1 may well indicate a role for PPT1 in the exocytotic pathway of neurons.

  16. was only detected in developing testis not ovary

  17. The severely affected PPT1-/- mouse CNS exhibited reduced volume of both cortical and subcortical regions, but with sparing of the cerebellum

  18. Autopsy of PPT1 mutant mice revealed a severe loss of brain mass and accumulation of autofluorescent granular osmiophilic deposits, both characteristic of Neuronal Ceroid Lipofuscinosis.

  19. We conclude that from an early age, neurons deficient in PPT1 enzyme activity display intrinsically abnormal properties that could potentially explain key features of the clinical disease, such as myoclonus and seizures.

  20. Palmitoyl-protein thioesterase-1 deficiency mediates the activation of the unfolded protein response and neuronal apoptosis in infantile neuronal ceroid lipofuscinosis.

PPT1 Antigen Profile

Protein Summary

The protein encoded by this gene is a small glycoprotein involved in the catabolism of lipid-modified proteins during lysosomal degradation. The encoded enzyme removes thioester-linked fatty acyl groups such as palmitate from cysteine residues. Defects in this gene are a cause of infantile neuronal ceroid lipofuscinosis 1 (CLN1, or INCL) and neuronal ceroid lipofuscinosis 4 (CLN4). Two transcript variants encoding different isoforms have been found for this gene.

Gene names and symbols associated with PPT1

  • palmitoyl-protein thioesterase 1 (PPT1) antibody
  • palmitoyl-protein thioesterase 1 (MGYG_00692) antibody
  • palmitoyl-protein thioesterase 1 (Ppt1) antibody
  • Palmitoyl-protein thioesterase 1 (ppt-1) antibody
  • palmitoyl-protein thioesterase 1 (ceroid-lipofuscinosis, neuronal 1, infantile) (ppt1) antibody
  • palmitoyl-protein thioesterase 1 L homeolog (ppt1.L) antibody
  • 9530043G02Rik antibody
  • AA960502 antibody
  • C77813 antibody
  • CLN1 antibody
  • D4Ertd184e antibody
  • INCL antibody
  • Ppt antibody
  • PPT-1 antibody
  • ppt1 antibody
  • wu:fj17f04 antibody
  • zgc:63969 antibody

Protein level used designations for PPT1

ceroid-palmitoyl-palmitoyl-protein thioesterase 1 , palmitoyl-protein hydrolase 1 , palmitoyl-protein thioesterase 1 , PPT-1 , palmitoyl-protein thioesterase 1 (ceroid-lipofuscinosis, neuronal 1, infantile) , palmitoyl protein thioesterase , Palmitoyl-protein hydrolase 1 , palmitoyl-protein thioesterase 1 L homeolog

GENE ID SPECIES
5538 Homo sapiens
10031925 Arthroderma gypseum CBS 118893
19063 Mus musculus
29411 Rattus norvegicus
419681 Gallus gallus
475316 Canis lupus familiaris
281421 Bos taurus
191744 Caenorhabditis elegans
406648 Danio rerio
100720295 Cavia porcellus
102126191 Macaca fascicularis
100037210 Xenopus laevis
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