Anti-Polyethylene glycol antibody [EPR21993-154] - BSA and Azide free (ab256481)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rabbit monoclonal [EPR21993-154] to Polyethylene glycol - BSA and Azide free
- Suitable for: WB, ELISA
- Reacts with: Species independent
Overview
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Product name
Anti-Polyethylene glycol antibody [EPR21993-154] - BSA and Azide free
See all Polyethylene glycol primary antibodies -
Description
Rabbit monoclonal [EPR21993-154] to Polyethylene glycol - BSA and Azide free -
Host species
Rabbit -
Tested applications
Suitable for: WB, ELISAmore details
Unsuitable for: IHC-P -
Species reactivity
Reacts with: Species independent -
Immunogen
Chemical/ Small Molecule. This information is proprietary to Abcam and/or its suppliers.
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Positive control
- WB: BSA-methoxy PEG 5K lysate.
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General notes
Ab256481 is the carrier-free version of ab203857. 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
ab256481 is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm.
Maxpar® is a trademark of Fluidigm Canada Inc.
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 production
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
Properties
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Form
Liquid -
Storage instructions
Shipped at 4°C. Store at +4°C. Do Not Freeze. -
Storage buffer
pH: 7.2
Constituent: PBS -
Carrier free
Yes -
Concentration information loading...
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Purity
Protein A purified -
Clonality
Monoclonal -
Clone number
EPR21993-154 -
Isotype
IgG -
Research areas
Images
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Direct ELISA antigen dose-response curve using AffniPure Goat Anti-Mouse IgG (H&L) at 1 µg/ml concentration. The detector antibody was ab203857 anti-Polyethylene glycol at 1 µg/ml. The secondary antibody was a Alkaline Phosphatase AffiniPure Goat Anti-Rabbit IgG (H+L) at 1/2500 dilution.
Antigen concentration range: 0-1000 ng/ml.
Blocking/Diluting Buffer and concentration: 1% BSA/TBS
Washing Buffer: 1 X TBST
Substrate: p-nitrophenyl phosphate (PNPP).
Coloration time: 10 min.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab203857).
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Direct ELISA antigen dose-response curve using ab203857 at 2 µg/ml concentration. The detector antibody was a anti-Polyethylene glycol antibody (Biotin) (ab53449) at 500 ng/ml. The secondary antibody was a Peroxidase-conjugated Streptavidin at 1/1000 dilution.
Antigen concentration range: 0-1000 ng/ml.
Blocking/Diluting Buffer and concentration: 1% BSA/TBS
Washing Buffer: 1 X TBST
Substrate: 3,3',5,5'-Tetramethylbenzidine (TMB).
Coloration time: 2 min.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab203857).
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Direct ELISA antigen dose-response curve using ab203857 at 2 µg/ml concentration. The detector antibody was a anti-Polyethylene glycol antibody (Biotin) (ab53449) at 500 ng/ml. The secondary antibody was a Peroxidase-conjugated Streptavidin at 1/1000 dilution.
Antigen concentration range: 0-1000 ng/ml.
Blocking/Diluting Buffer and concentration: 1% BSA/TBS
Washing Buffer: 1 X TBST
Substrate: 3,3',5,5'-Tetramethylbenzidine (TMB).
Coloration time: 2 min.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab203857).
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Direct ELISA antigen dose-response curve using ab203857 at 0.05 µg/ml concentration. The secondary antibody was a Alkaline Phosphatase AffiniPure Goat Anti-Rabbit IgG (H+L) at 1/2500 dilution.
Antigen concentration range: 0-0.05µg/ml.
Blocking/Diluting Buffer and concentration: 1% BSA/TBS
Washing Buffer: 1 X TBST
Substrate: p-nitrophenyl phosphate (PNPP).
Coloration time: 15 min.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab203857).
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Direct ELISA antigen dose-response curve using ab203857 at 0.05 µg/ml concentration. The secondary antibody was a Alkaline Phosphatase AffiniPure Goat Anti-Rabbit IgG (H+L) at 1/2500 dilution.
Antigen concentration range: 0-0.05µg/ml.
Blocking/Diluting Buffer and concentration: 1% BSA/TBS
Washing Buffer: 1 X TBST
Substrate: p-nitrophenyl phosphate (PNPP).
Coloration time: 15 min.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab203857).
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Functional Studies - Anti-Polyethylene glycol antibody [EPR21993-154] - BSA and Azide free (ab256481)
Method: APS sensor+ Antigen (methoxy PEG800 at 0.625 µg/ml) + Blocking (BSA) + Antibody (ab203857 at2, 1, 0.5, 0.25, 0.125ug/ml).
Results:
KD (M) = 5.81E-11
kon(1/Ms) = 2.70E+05
kon Error = 6.28E+02
kdis(1/s) = 1.57E-05
kdis Error = 4.49E-07
Full X2= 10.143
Full R2= 0.9993
Testing Biosensor: Aminopropylsilane (APS) Biosensors
Testing machine: Fortebio RED96e
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab203857).
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Functional Studies - Anti-Polyethylene glycol antibody [EPR21993-154] - BSA and Azide free (ab256481)
Method: APS sensor+ Antigen (methoxy PEG800 at 25 µg/ml) + Blocking (BSA) + Antibody (ab203857 at 0.5, 0.25, 0.125, 0.0625, 0.03125ug/ml).
Results:
KD (M) = 1.29E-10
kon(1/Ms) = 2.23E+06
kon Error = 1.45E+04
kdis(1/s) = 2.88E-04
kdis Error = 1.74E-06
Full X^2 = 3.475
Full R^2 = 0.9865
Testing Biosensor: Aminopropylsilane (APS) Biosensors
Testing machine: Fortebio RED96e
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab203857).
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