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Read our guarantee »Products:Cardiovascular >> Lipids / Lipoproteins >> Adipose Related >> Lipid Droplet Protein
Anti-Perilipin A antibody
See all Perilipin A products (6) ...
Rabbit polyclonal to Perilipin A
IHC-P, WB, IHC-FoFr, ICC/IFmore details
Reacts with
Mouse, Rhesus monkey
Predicted to work with
Rat, Human
Synthetic Peptide: CE(502)PILGRTQYSQLRKKS(517). Immunizing peptide corresponds to amino acid residues 502-517 from rat Perilipin A. This sequence is 93% conserved in humans.
C-EPILGRTQ YSQLRKKS
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
PBS with 0.05% sodium azide
Concentration information loading...
Immunogen affinity purified
Adipose tissue is an energy reserve in animals and is strictly regulated in nondomestic species. Adipose cells produce and secrete numerous physiologically important proteins, such as lipoprotein lipase (LPL), leptin, adipocyte complement related protein of 30 kDa (Acrp30), resistin, and Perilipin. Perilipin is an intracellular neutral lipid droplet protein that is hormonally regulated. This protein is localized exclusively to the surface of lipid droplets. In response to lypotic stimuli, Perilipin is phosphorylated by protein kinase A. Once activated, Perilipin has inhibitory affects upon hormone-sensitive lipase (HSL), a protein that mediates the hydrolysis of triacylglycerol, the major form of stored energy in the body. Perilipin expression is limited to adipocytes and steroidogenic cells. There are currently two known isoforms, Perilipin A and B. Both of these proteins are encoded by a single-copy gene and are the result of differential splicing events.
Polyclonal
IgG
Cancer >> Cancer Metabolism >> Metabolic signaling pathway >> Metabolism of lipids and lipoproteins
Cardiovascular >> Atherosclerosis >> Lipoprotein metabolism
Signal Transduction >> Metabolism >> Lipid metabolism
Cardiovascular >> Lipids / Lipoproteins >> Adipose Related >> Lipid Droplet Protein
Our Abpromise guarantee covers the use of ab3526 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
IHC-P: Use at an assay dependent dilution. Perform heat mediated antigen retrieval before commencing with IHC staining protocol.
WB: Use at an assay dependent dilution. (By Western blot, this antibody detects an ~62 kDa protein representing Perilipin A from 3T3-L1 cell extract)
IHC-FoFr: Use at an assay dependent dilution. (PubMed: 20049087)
ICC/IF: Use at an assay dependent dilution.
Modulator of adipocyte lipid metabolism. Coats lipid storage droplets to protect them from breakdown by hormone-sensitive lipase (HSL). Its absence may result in leanness.
Adipocytes.
Belongs to the perilipin family.
Major cAMP-dependent protein kinase-substrate in adipocytes, also dephosphorylated by PP1. When phosphorylated, may be maximally sensitive to HSL and when unphosphorylated, may play a role in the inhibition of lipolysis, by acting as a barrier in lipid droplet.
Lipid droplet. Lipid droplet surface-associated.
Target information above from: UniProt accessionO60240
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - Perilipin A antibody (ab3526)

Western blot of perilipin A in 3T3-L1 cell extract using ab3526.
Immunocytochemistry/ Immunofluorescence - Perilipin A antibody (ab3526)

ab3526 staining Perilipin A in rat myofibers by Immunohistochemistry (PFA fixed).Freshly isolated single myofibers were collected in 0.5 ml DMEM, 5% HS in an Eppendorf tube. Fibers and satellite cells were fixed with 4% paraformaldehyde in phosphate buffered saline, rinsed in PBS and permeabilized with Triton X-100, 0.5% in PBS. After washing, fibers and/or cells were incubated with ab3526 at a 1/50 dilution overnight at 4°C or 1 hour at 37°C. Non specific interactions were blocked with 20% goat serum. They were then washed and incubated with labeled secondary antibodies for one hour at room temperature. Satellite cells were then mounted with fluorescent mounting medium plus DAPI 100 ng/ml. Fibers were collected and moved onto a polilysine microscope slide, and then mounted.
Image from Rossi CA et al, PLoS One. 2010 Jan 1;5(1):e8523, Fig 3.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Perilipin A antibody (ab3526)

ab3526 (4µg/ml) staining perilipin in human breast adipose using an automated system (DAKO Autostainer Plus). Using this protocol there is strong cytoplasmic staining of adipocytes.
Sections were rehydrated and antigen retrieved with the Dako 3 in 1 AR buffer citrate pH6.1 in a DAKO PT link. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 mins. They were then blocked with Dako Protein block for 10 minutes (containing casein 0.25% in PBS) then incubated with primary antibody for 20 min and detected with Dako envision flex amplification kit for 30 minutes. Colorimetric detection was completed with Diaminobenzidine for 5 minutes. Slides were counterstained with Haematoxylin and coverslipped under DePeX. Please note that, for manual staining, optimization of primary antibody concentration and incubation time is recommended. Signal amplification may be required.
This product has been referenced in:
See all 6 publications for this product
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Western blot of perilipin A in 3T3-L1 cell extract using ab3526.

ab3526 staining Perilipin A in rat myofibers by Immunohistochemistry (PFA fixed).Freshly isolated single myofibers were collected in 0.5 ml DMEM, 5% HS in an Eppendorf tube. Fibers and satellite cells were fixed with 4% paraformaldehyde in phosphate buffered saline, rinsed in PBS and permeabilized with Triton X-100, 0.5% in PBS. After washing, fibers and/or cells were incubated with ab3526 at a 1/50 dilution overnight at 4°C or 1 hour at 37°C. Non specific interactions were blocked with 20% goat serum. They were then washed and incubated with labeled secondary antibodies for one hour at room temperature. Satellite cells were then mounted with fluorescent mounting medium plus DAPI 100 ng/ml. Fibers were collected and moved onto a polilysine microscope slide, and then mounted.
Image from Rossi CA et al, PLoS One. 2010 Jan 1;5(1):e8523, Fig 3.

ab3526 (4µg/ml) staining perilipin in human breast adipose using an automated system (DAKO Autostainer Plus). Using this protocol there is strong cytoplasmic staining of adipocytes.
Sections were rehydrated and antigen retrieved with the Dako 3 in 1 AR buffer citrate pH6.1 in a DAKO PT link. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 mins. They were then blocked with Dako Protein block for 10 minutes (containing casein 0.25% in PBS) then incubated with primary antibody for 20 min and detected with Dako envision flex amplification kit for 30 minutes. Colorimetric detection was completed with Diaminobenzidine for 5 minutes. Slides were counterstained with Haematoxylin and coverslipped under DePeX. Please note that, for manual staining, optimization of primary antibody concentration and incubation time is recommended. Signal amplification may be required.
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