Rabbit Polyclonal PPT1/PPT antibody. Suitable for IHC-P, WB and reacts with Mouse, Rat, Human samples. Cited in 1 publication. Immunogen corresponding to Recombinant Fragment Protein within Human PPT1 aa 1 to C-terminus.
pH: 7
Preservative: 0.01% Thimerosal (merthiolate)
Constituents: 10% Glycerol (glycerin, glycerine), 1.21% Tris, 0.75% Glycine
IHC-P | WB | |
---|---|---|
Human | Tested | Tested |
Mouse | Tested | Expected |
Rat | Tested | Expected |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info 1/100.00000 - 1/1000.00000 | Notes Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Species Rat | Dilution info 1/100.00000 - 1/1000.00000 | Notes Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Species Human | Dilution info 1/100.00000 - 1/1000.00000 | Notes Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/500.00000 - 1/3000.00000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info Use at an assay dependent concentration. | Notes - |
Select an associated product type
Removes thioester-linked fatty acyl groups such as palmitate from modified cysteine residues in proteins or peptides during lysosomal degradation. Prefers acyl chain lengths of 14 to 18 carbons (PubMed:8816748).
CLN1, PPT, PPT1, Palmitoyl-protein thioesterase 1, PPT-1, Palmitoyl-protein hydrolase 1
Rabbit Polyclonal PPT1/PPT antibody. Suitable for IHC-P, WB and reacts with Mouse, Rat, Human samples. Cited in 1 publication. Immunogen corresponding to Recombinant Fragment Protein within Human PPT1 aa 1 to C-terminus.
pH: 7
Preservative: 0.01% Thimerosal (merthiolate)
Constituents: 10% Glycerol (glycerin, glycerine), 1.21% Tris, 0.75% Glycine
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PPT1 also known as palmitoyl-protein thioesterase 1 is an enzyme that plays a critical role in protein metabolism by removing thioester-linked palmitate groups from proteins. This enzyme has a molecular weight of approximately 37 kDa. PPT1 is expressed widely in the body with significant expression in tissues such as the brain and liver. It localizes primarily in the lysosomes where it assists in lysosomal degradation pathways. Polyclonal antibodies against PPT1 can be utilized in protein analysis and help elucidate the structure and functionality of this enzyme further.
PPT1 contributes to the turnover and stability of proteins by mediating their de-palmitoylation an important step in maintaining appropriate protein function and cellular homeostasis. This enzyme assists in the recycling and degradation process by facilitating the catabolism of proteins through the lysosomal pathway. PPT1 does not function as part of a larger complex but operates individually to execute the removal of palmitate which impacts a diverse range of substrates vital for controlling cellular mechanisms such as synaptic function.
PPT1 is heavily involved in the protein degradation pathway within lysosomes. This pathway is important for the autophagic degradation process which directly associates with cellular waste management and the recycling of cellular components. PPT1's function is also connected to protein stability because improper palmitoylation can disrupt protein location and function. The enzyme shows functional interaction with proteins like CLN2 which also participates in lysosomal degradation processes and they share involvement in neuronal homeostasis.
Defects in PPT1 activity lead to neurodegenerative conditions notably the Infantile Neuronal Ceroid Lipofuscinosis (INCL). This disorder results from the accumulation of lipid-protein complexes in neurons emphasizing the need for proper PPT1 function. PPT1 has connections to the disease context through its interaction with the protein CLN3 another gene implicated in Batten disease part of the neuronal ceroid lipofuscinoses group. The study of PPT1 opens avenues for therapeutic approaches targeting these lysosomal storage disorders. Immunohistochemistry and immunocytochemistry are techniques often used to study the role of PPT1 in these pathological states.
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Immunohistochemical analysis of paraffin-embedded CL1-0 (human) xenograft tissue staining PPT1 with ab137578 at 1/500 dilution. EDTA based antigen retrieval pH 8.0 for 15 mins.
10% SDS-PAGE
All lanes: Western blot - Anti-PPT1/PPT antibody (ab137578) at 1/1000 dilution
All lanes: Raji (human Burkitt's lymphoma cell line) whole cell lysate at 30 µg
All lanes: HRP-conjugated anti-rabbit IgG antibody
Predicted band size: 34 kDa
Immunohistochemical analysis of paraffin-embedded mouse stomach tissue staining PPT1 at lysosome with ab137578 at 1/500 dilution. EDTA based antigen retrieval pH 8.0 for 15 mins.
Immunohistochemical analysis of paraffin-embedded rat hind brain tissue staining PPT1 at lysosome with ab137578 at 1/500 dilution. EDTA based antigen retrieval pH 8.0 for 15 mins.
Immunohistochemical analysis of paraffin-embedded mouse fore brain tissue staining PPT1 at lysosome with ab137578 at 1/500 dilution. EDTA based antigen retrieval pH 8.0 for 15 mins.
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