Anti-DDR2 antibody [EPR18826-119] - BSA and Azide free (ab280369)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rabbit monoclonal [EPR18826-119] to DDR2 - BSA and Azide free
- Suitable for: WB
- Reacts with: Mouse, Rat, Human
Overview
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Product name
Anti-DDR2 antibody [EPR18826-119] - BSA and Azide free
See all DDR2 primary antibodies -
Description
Rabbit monoclonal [EPR18826-119] to DDR2 - BSA and Azide free -
Host species
Rabbit -
Tested applications
Suitable for: WBmore details
Unsuitable for: Flow Cyt,ICC,IHC-P or IP -
Species reactivity
Reacts with: Mouse, Rat, Human -
Immunogen
Recombinant fragment. This information is proprietary to Abcam and/or its suppliers.
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Positive control
- WB: HT-1080, HUVEC, A-204, A375, Human stomach, ovary, lung, Mouse ovary, lung, C2C12, C6, Rat ovary and His-tagged human DDR2 recombinant protein (aa22-399).
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General notes
ab280369 is the carrier-free version of ab280354. 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
ab280369 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. -
Storage buffer
Constituent: 100% PBS -
Carrier free
Yes -
Concentration information loading...
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Purity
Protein A purified -
Clonality
Monoclonal -
Clone number
EPR18826-119 -
Isotype
IgG -
Research areas
Images
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All lanes : Anti-DDR2 antibody [EPR18826-119] (ab280354) at 1/1000 dilution
Lane 1 : HT-1080 (human fibrosarcoma epithelial cell) whole cell lysate
Lane 2 : HUVEC (human umbilical vein endothelial cell) whole cell lysate
Lane 3 : A-204 (rat muscle rhabdomyosarcoma) whole cell lysate
Lane 4 : A375 (human malignant melanoma epithelial cell) whole cell lysate
Lane 5 : MDA-MB-231 (human breast adenocarcinoma epithelial cell) whole cell lysate
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution (Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated)
Predicted band size: 97 kDa
Observed band size: 120-130,70 kDa why is the actual band size different from the predicted?This data was developed using ab280354, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: 5% NFDM/TBST
This blot was developed using a higher sensitivity ECL substrate.
The expression pattern is consistent with what has been described in the literature (PMID: 15111304, 29616590).
Negative control: MDA-MB-231 (PMID: 28147276, 29616590)
Exposure time: 158 seconds.
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All lanes : Anti-DDR2 antibody [EPR18826-119] (ab280354) at 1/1000 dilution
Lane 1 : Human stomach tissue lysate
Lane 2 : Human ovary tissue lysate
Lane 3 : Human lung tissue lysate
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Predicted band size: 97 kDa
Observed band size: 120-130,70 kDa why is the actual band size different from the predicted?This data was developed using ab280354, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: 5% NFDM/TBST
The expression pattern is consistent with what has been described in the literature (PMID: 15111304, 29616590).
Exposure time: 3 minutes.
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All lanes : Anti-DDR2 antibody [EPR18826-119] (ab280354) at 1/1000 dilution
Lane 1 : Mouse ovary tissue lysate
Lane 2 : Mouse lung tissue lysate
Lane 3 : C2C12 (mouse myoblasts myoblast) whole cell lysate
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution (Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated)
Predicted band size: 97 kDa
Observed band size: 120-130,70 kDa why is the actual band size different from the predicted?This data was developed using ab280354, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: 5% NFDM/TBST
The expression pattern is consistent with what has been described in the literature (PMID: 15111304, 29616590).
Exposure time: 3 minutes.
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All lanes : Anti-DDR2 antibody [EPR18826-119] (ab280354) at 1/1000 dilution
Lane 1 : C6 (rat glial tumor glial cell) whole cell lysate
Lane 2 : Rat ovary tissue lysate
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution (Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated)
Predicted band size: 97 kDa
Observed band size: 120-130,70 kDa why is the actual band size different from the predicted?This data was developed using ab280354, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: 5% NFDM/TBST
The expression pattern is consistent with what has been described in the literature (PMID: 15111304, 29616590).
Exposure time: 3 minutes
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All lanes : Anti-DDR2 antibody [EPR18826-119] (ab280354) at 1/1000 dilution
Lane 1 : His-tagged human DDR2 recombinant protein (aa22-399)
Lane 2 : His-tagged human DDR1 recombinant protein (aa21-416)
Lysates/proteins at 0.03 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution (Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated)
Predicted band size: 97 kDa
Observed band size: 60 kDa why is the actual band size different from the predicted?This data was developed using ab280354, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: 5% NFDM/TBST
This antibody can not recognize human DDR1.
Both recombinant proteins are made in house and extracted from HEK-293 expression systems.
Exposure time: 8 seconds.
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