Anti-Aurora A antibody [EPR5026] - BSA and Azide free (ab247643)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rabbit monoclonal [EPR5026] to Aurora A - BSA and Azide free
- Suitable for: ICC/IF, Flow Cyt, IP, WB
- Reacts with: Mouse, Human
Overview
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Product name
Anti-Aurora A antibody [EPR5026] - BSA and Azide free
See all Aurora A primary antibodies -
Description
Rabbit monoclonal [EPR5026] to Aurora A - BSA and Azide free -
Host species
Rabbit -
Tested applications
Suitable for: ICC/IF, Flow Cyt, IP, WBmore details
Unsuitable for: IHC-P -
Species reactivity
Reacts with: Mouse, Human -
Immunogen
Synthetic peptide. This information is proprietary to Abcam and/or its suppliers.
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General notes
ab247643 is the carrier-free version of ab108353 This format is designed for use in antibody labeling, including fluorochromes, metal isotopes, oligonucleotides, enzymes.
Our carrier-free formats are supplied in a buffer free of BSA, sodium azide and glycerol for higher conjugation efficiency.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with
Ab247643 is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm.
Maxpar® is a trademark of Fluidigm Canada Inc.
Rat: We have preliminary internal testing data to indicate this antibody may not react with this species. Please contact us for more information.
Properties
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Form
Liquid -
Storage instructions
Shipped at 4°C. Store at +4°C. Do Not Freeze. -
Dissociation constant (KD)
KD = 2.63 x 10 -10 M Learn more about KD -
Storage buffer
pH: 7.2
Constituent: PBS -
Carrier free
Yes -
Concentration information loading...
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Purity
Affinity purified -
Clonality
Monoclonal -
Clone number
EPR5026 -
Isotype
IgG -
Research areas
Images
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All lanes : Anti-Aurora A antibody [EPR5026] - Centrosome Marker (ab108353) at 1/1000 dilution
Lane 1 : BXPC-3 cell lysate
Lane 2 : LnCaP cell lysate
Lane 3 : SKBR-3 cell lysate
Lane 4 : HepG2 cell lysate
Lysates/proteins at 10 µg per lane.
Predicted band size: 46 kDaThis data was developed using ab108353, the same antibody clone in a different buffer formulation.
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This data was developed using ab108353, the same antibody clone in a different buffer formulation.Lane 1: Neuro2a (Mouse neuroblastoma neuroblast) whole cell lysate, 10µg
Lane 2: Neuro2a cell lysate 350µg and ab109518 2µg
Lane 3: Neuro2a cell lysate, 350µg and rabbit IgG (ab172730) , 2µg Purified ab108353 immunoprecipitating Aurora A in Neuro2a cell lysates. Primary antibody was used at a 1/60 dilution (20 µg/ml). For western blotting, ab108353 at 1/500 and VeriBlot for IP Detection Reagent (HRP) (ab131366), was used for detection at 1/1000 dilution. Blocking and diluting buffer used: 5% NFDM/TBST. -
This data was developed using ab108353, the same antibody clone in a different buffer formulation.Lane 1: HepG2 (Human hepatocellular carcinoma epithelial cell) whole cell lysate 10µg
Lane 2: HepG2 cell lysate 350µg and ab109518 2µg
Lane 3: HepG2 cell lysate 350µg and rabbit IgG (ab172730) , 2µg
Purified ab108353 immunoprecipitating Aurora A in Neuro2a cell lysates. Primary antibody was used at a 1/60 dilution (20 µg/ml). For western blotting, ab108353 at 1/500 and VeriBlot for IP Detection Reagent (HRP) (ab131366), was used for detection at 1/1000 dilution. Blocking and diluting buffer used: 5% NFDM/TBST. -
This data was developed using ab108353, the same antibody clone in a different buffer formulation.Overlay histogram showing HeLa cells stained with ab108353 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab108353, 1/1000 dilution) for 30 min at 22°C. The secondary antibody used was Alexa Fluor® 488 goat anti-rabbit IgG (H&L) (ab150077) at 1/2000 dilution for 30 min at 22°C. Isotype control antibody (black line) was rabbit IgG (monoclonal) (0.1?g/1x106 cells) used under the same conditions. Unlabelled sample (blue line) was also used as a control. Acquisition of >5,000 events were collected using a 20mW Argon ion laser (488nm) and 525/30 bandpass filter.
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This data was developed using ab108353, the same antibody clone in a different buffer formulation.Equilibrium disassociation constant (KD)
Learn more about KD
Click here to learn more about KD
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