Anti-Cytosolic Phospholipase A2 antibody [EPR26068-26] - BSA and Azide free
- RabMAb
- Recombinant
- KO Validated
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Knockout Tested Rabbit Recombinant Monoclonal Cytosolic Phospholipase A2 antibody. Carrier free. Suitable for WB, IP and reacts with Human, Mouse, Rat samples.
View Alternative Names
CPLA2, PLA2G4, PLA2G4A, Cytosolic phospholipase A2, cPLA2, Phospholipase A2 group IVA
- IP
Supplier Data
Immunoprecipitation - Anti-Cytosolic Phospholipase A2 antibody [EPR26068-26] - BSA and Azide free (AB307890)
This data was produced using ab307889 the same antibody clone but in a different buffer. Cytosolic Phospholipase A2 was immunoprecipitated from 0.35 mg HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate 10 ug with ab307889 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab307889 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution. Lane 1 : HeLa whole cell lysate 10 ug Lane 2 : ab307889 IP in HeLa whole cell lysate Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab307889 in HeLa whole cell lysate Blocking and dilution buffer and concentration : 5% NFDM/TBST. Exposure time : 50 seconds.
All lanes:
Immunoprecipitation - Anti-Cytosolic Phospholipase A2 antibody [EPR26068-26] (<a href='/en-us/products/primary-antibodies/cytosolic-phospholipase-a2-antibody-epr26068-26-ab307889'>ab307889</a>) at 1/30 dilution
All lanes:
<a href='/en-us/products/primary-antibodies/cytosolic-phospholipase-a2-antibody-epr26068-26-ab307889'>ab307889</a> IP in HeLa whole cell lysate at 10 µg
false
Exposure time: 50s
- WB
Supplier Data
Western blot - Anti-Cytosolic Phospholipase A2 antibody [EPR26068-26] - BSA and Azide free (AB307890)
This data was produced using ab307889 the same antibody clone but in a different buffer. In lane 1, the lysate was freshly made and used for Western Blotting immediately to minimize protein degradation. In lanes 2-3, the lysates were stored at -80℃ prior to Western Blotting. The bands beneath the target band (75 kDa) are likely to be degradation products. The secondary antibody dilution for Lane1 was 1 : 100000, the secondary antibody dilution for Lane2 and 3 was 1 : 20000. In Western blot, anti-GAPDH antibody (ab181602) loading control staining at 1/200000 dilution. Blocking/Dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-Cytosolic Phospholipase A2 antibody [EPR26068-26] (<a href='/en-us/products/primary-antibodies/cytosolic-phospholipase-a2-antibody-epr26068-26-ab307889'>ab307889</a>) at 1/1000 dilution
Lane 1:
HeLa whole cell lysate at 20 µg
Lane 2:
HeLa transfected with scrambled siRNA control whole cell lysate at 20 µg
Lane 3:
HeLa transfected with siRNA specifically targeting Cytosolic Phospholipase A2 whole cell lysate at 20 µg
Secondary
Lane 1:
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 1/100000 dilution
Lanes 2 - 3:
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
Predicted band size: 85 kDa
Observed band size: 100 kDa
false
- WB
Supplier Data
Western blot - Anti-Cytosolic Phospholipase A2 antibody [EPR26068-26] - BSA and Azide free (AB307890)
This data was produced using ab307889 the same antibody clone but in a different buffer. Lysates at 20 µg per lane. The samples were run on a Bis-Tris gel. Performed under reducing conditions. False colour image of Western blot : Anti-Cytosolic Phospholipase A2 antibody (ab307889) staining at 1/1000 dilution, shown in green; Mouse anti-GAPDH antibody 6C5 (ab8245) loading control staining at 1/20000 dilution, shown in red. In Western blot, ab307889 was shown to bind specifically to Cytosolic Phospholipase A2. A band was observed at 100 kDa in wild-type HAP1 cell lysates with no signal observed at this size in Cytosolic Phospholipase A2 knockout cell line. To generate this image, wild-type and Cytosolic Phospholipase A2 knockout HAP1 cell lysates were analyzed. First, samples were run on an SDS-PAGE gel then transferred onto an immobilon-FL PVDF membrane. Membranes were blocked in in Intercept® (TBS) Blocking Buffer diluted with an equal volume of 0.1% TBS before incubation with primary antibodies overnight at 4 °C. Blots were washed four times in TBS-T, incubated with secondary antibodies for 1 h at room temperature, washed again four times then imaged. Secondary antibodies used were Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed (ab216776) at 1/20000 dilution. The identity of the lower MW band at approximately 75 kDa is unknown.
All lanes:
Western blot - Anti-Cytosolic Phospholipase A2 antibody [EPR26068-26] (<a href='/en-us/products/primary-antibodies/cytosolic-phospholipase-a2-antibody-epr26068-26-ab307889'>ab307889</a>) at 1/1000 dilution
Lane 1:
Wild-type HAP1 whole cell lysate at 20 µg
Lane 2:
Cytosolic Phospholipase A2 knockout HAP1 whole cell lysate at 20 µg
Lane 3:
HeLa whole cell lysate at 20 µg
Lane 4:
A549 whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-irdye-800cw-preadsorbed-ab216773'>ab216773</a>) at 1/10000 dilution
Predicted band size: 85 kDa
Observed band size: 100 kDa
false
- WB
Lab
Western blot - Anti-Cytosolic Phospholipase A2 antibody [EPR26068-26] - BSA and Azide free (AB307890)
This data was developed using ab312848, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602).
In Western blot, ab307889 was shown to bind specifically to Cytosolic Phospholipase A2. A band was observed at 100 kDa in wild-type HeLa cell lysates with no signal observed at this size in Cytosolic Phospholipase A2 knockout cell line(lane 2) (lane 2, knockout cell line ab265490 / knockout cell lysate ab257133).
All lanes:
Western blot - Anti-Cytosolic Phospholipase A2 antibody [EPR26068-26] (<a href='/en-us/products/primary-antibodies/cytosolic-phospholipase-a2-antibody-epr26068-26-ab307889'>ab307889</a>) at 1/1000 dilution
Lane 1:
Wild-type HeLa (human cervical adenocarcinoma epithelial cell) whole cell lysate at 20 µg
Lane 2:
Cytosolic Phospholipase A2 knockout HeLa whole cell lysate at 20 µg
Lane 2:
Western blot - Human PLA2G4A (Cytosolic Phospholipase A2) knockout HeLa cell line (<a href='/en-us/products/cell-lines/human-pla2g4a-cytosolic-phospholipase-a2-knockout-hela-cell-line-ab265490'>ab265490</a>)
Lane 2:
Western blot - Human PLA2G4A (Cytosolic Phospholipase A2) knockout HeLa cell lysate (<a href='/en-us/products/cell-lysates/human-pla2g4a-cytosolic-phospholipase-a2-knockout-hela-cell-lysate-ab257133'>ab257133</a>) 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 1/100000 dilution
Observed band size: 100 kDa
false
Exposure time: 38s
- WB
Supplier Data
Western blot - Anti-Cytosolic Phospholipase A2 antibody [EPR26068-26] - BSA and Azide free (AB307890)
This data was produced using ab307889 the same antibody clone but in a different buffer. Lane 3 was developed using a high sensitivity ECL substrate. In Western blot, anti-GAPDH antibody (ab181602) loading control staining at 1/200000 dilution. Blocking/Dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-Cytosolic Phospholipase A2 antibody [EPR26068-26] (<a href='/en-us/products/primary-antibodies/cytosolic-phospholipase-a2-antibody-epr26068-26-ab307889'>ab307889</a>) at 1/1000 dilution
Lane 1:
NIH/3T3 whole cell lysate at 20 µg
Lane 2:
RAW264.7 whole cell lysate at 20 µg
Lane 3:
C6 whole cell lysate 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 1/100000 dilution
Predicted band size: 85 kDa
Observed band size: 100 kDa
true
Reactivity data
Product details
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
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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