Anti-Adipose Triglyceride Lipase (phospho S406) antibody [EPR27159-29] - BSA and Azide free
- Recombinant
- RabMAb
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Rabbit Recombinant Monoclonal Adipose Triglyceride Lipase phospho S406 antibody. Carrier free. Suitable for I-ELISA, WB, IP, ICC/IF and reacts with Synthetic peptide - Human, Synthetic peptide - Mouse, Mouse, Human samples.
View Alternative Names
Atgl, Pnpla2, Patatin-like phospholipase domain-containing protein 2, Adipose triglyceride lipase, Calcium-independent phospholipase A2-zeta, Desnutrin, iPLA2-zeta
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-Adipose Triglyceride Lipase (phospho S406) antibody [EPR27159-29] - BSA and Azide free (AB317611)
This data was developed using ab317610, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized 3T3-L1 (mouse embryonic fibroblast) cells labelling Adipose Triglyceride Lipase with ab317610 at 1/50 (10.08 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2 ug/ml dilution (Green).
Confocal image showing cytoplasmic and membranous staining in differentiated 3T3-L1 cells (shown in green). The counterstain was observed in magenta. Nuclear DNA was labeled with DAPI (shown in blue).
Image was taken with a confocal microscope(Leica-Microsystems, TCS SP8).
ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 2.5ug/ml dilution (Magenta). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/ml dilution.
- IP
Supplier Data
Immunoprecipitation - Anti-Adipose Triglyceride Lipase (phospho S406) antibody [EPR27159-29] - BSA and Azide free (AB317611)
This data was developed using ab317610, the same antibody clone in a different buffer formulation.
Adipose Triglyceride Lipase was immunoprecipitated from 0.35 mg Differentiated 3T3-L1(mouse embryonic fibroblast) for 6 days whole cell lysate with ab317610 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab317610 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : Differentiated 3T3-L1(mouse embryonic fibroblast) for 6 days whole cell lysate
Lane 2 : ab317610 IP in Differentiated 3T3-L1(mouse embryonic fibroblast) for 6 days whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab317610 in differentiated 3T3-L1 for 6 days whole cell lysate
All lanes:
Immunoprecipitation - Anti-Adipose Triglyceride Lipase (phospho S406) antibody [EPR27159-29] (<a href='/en-us/products/primary-antibodies/adipose-triglyceride-lipase-phospho-s406-antibody-epr27159-29-ab317610'>ab317610</a>) at 1/30 dilution
All lanes:
Differentiated 3T3-L1(mouse embryonic fibroblast) for 6 days whole cell lysate at 10 µg
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
false
Exposure time: 180s
- WB
Lab
Western blot - Anti-Adipose Triglyceride Lipase (phospho S406) antibody [EPR27159-29] - BSA and Azide free (AB317611)
This data was developed using ab317610, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST
Exposure time :
Lane 1-2 : 5 seconds;
Lane 3-4 : 180 seconds
ab181602 was used as a GAPDH loading control at 1/200000 dilution
All lanes:
Western blot - Anti-Adipose Triglyceride Lipase (phospho S406) antibody [EPR27159-29] (<a href='/en-us/products/primary-antibodies/adipose-triglyceride-lipase-phospho-s406-antibody-epr27159-29-ab317610'>ab317610</a>) at 1/1000 dilution
Lane 1:
Human colon tissue lysate (untreated membrane) at 20 µg
Lane 2:
Human colon tissue lysate (Alkaline phosphatase treated membrane) at 20 µg
Lane 3:
Human fat tissue lysate (untreated membrane) at 20 µg
Lane 4:
Human fat tissue lysate (Alkaline phosphatase treated membrane) at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Observed band size: 55 kDa
false
- WB
Supplier Data
Western blot - Anti-Adipose Triglyceride Lipase (phospho S406) antibody [EPR27159-29] - BSA and Azide free (AB317611)
This data was developed using ab317610, the same antibody clone in a different buffer formulation.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
All lanes:
Western blot - Anti-Adipose Triglyceride Lipase (phospho S406) antibody [EPR27159-29] (<a href='/en-us/products/primary-antibodies/adipose-triglyceride-lipase-phospho-s406-antibody-epr27159-29-ab317610'>ab317610</a>) at 1/1000 dilution
Lane 1:
Undifferentiated 3T3-L1 (mouse embryonic fibroblast) whole cell lysate (untreated membrane) at 40 µg
Lane 2:
3T3-L1 differentiated for 6 days whole cell lysate (untreated membrane) at 40 µg
Lane 3:
Undifferentiated 3T3-L1 whole cell lysate (Lambda phosphatase treated membrane) at 40 µg
Lane 4:
3T3-L1 differentiated for 6 days whole cell lysate (Lambda phosphatase treated membrane) at 40 µg
Lane 5:
Mouse white fat tissue lysate (untreated membrane) at 40 µg
Lane 6:
Mouse white fat tissue lysate (Lambda phosphatase treated membrane) at 40 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Observed band size: 55 kDa,36 kDa
false
Exposure time: 180s
- ELISA
Supplier Data
ELISA - Anti-Adipose Triglyceride Lipase (phospho S406) antibody [EPR27159-29] - BSA and Azide free (AB317611)
This data was developed using ab317610, the same antibody clone in a different buffer formulation.
Indirect ELISA analysis of ab317610 at 1000-0 ng/ml. The Secondary antibody used was Alkaline Phosphatase-conjugated AffiniPure Goat Anti-Rabbit IgG (H+L) at 1 : 2500 dilution.
Antigen : Mouse Adipose Triglyceride Lipase(phospho S406),Mouse Adipose Triglyceride Lipase non-phospho,Mouse Adipose Triglyceride Lipase(mutated S406A), Human Adipose Triglyceride Lipase(phospho S404),Human Adipose Triglyceride Lipase non-phospho.
Antigen concentration : 100ng/ml
Related conjugates and formulations (1)
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Anti-Adipose Triglyceride Lipase (phospho S406) antibody [EPR27159-29]
Reactivity data
Product details
ab317611 is the carrier-free version of ab317610.
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
ATGL is part of the lipid mobilization process and contributes significantly to energy homeostasis. It acts distinctively as it breaks down phosphotriglycerides and is not part of a larger complex carrying out its function independently. Its activity impacts the balance of lipid storage and release important for maintaining energy levels within cells and across the entire organism.
Pathways
ATGL plays a significant role in the lipid catabolism and energy regulation pathways. ATGL's activity regulates the fat mobilization pathway by interacting closely with the protein Comparative Gene Identification-58 (CGI-58) which activates it. Further ATGL is involved in the peroxisome proliferator-activated receptor (PPAR) pathway highlighting its role in influencing metabolic processes and energy balance.
Product protocols
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Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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