Anti-pan-myc antibody [EPR18863] - BSA and Azide free (ab251199)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rabbit monoclonal [EPR18863] to pan-myc - BSA and Azide free
- Suitable for: WB, Flow Cyt, ICC/IF
- Reacts with: Mouse, Human
Overview
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Product name
Anti-pan-myc antibody [EPR18863] - BSA and Azide free
See all pan-myc primary antibodies -
Description
Rabbit monoclonal [EPR18863] to pan-myc - BSA and Azide free -
Host species
Rabbit -
Tested applications
Suitable for: WB, Flow Cyt, ICC/IFmore details -
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
Ab251199 is the carrier-free version of ab195207. 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
ab251199 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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Clonality
Monoclonal -
Clone number
EPR18863 -
Isotype
IgG -
Research areas
Images
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All lanes : Anti-pan-myc antibody [EPR18863] (ab195207) at 1/5000 dilution
Lane 1 : HEK-293 (Human epithelial cells from embryonic kidney) whole cell lysate transfected with empty vector (vector control)
Lane 2 : HEK-293 whole cell lysate transfected with n-Myc with GFP-tag
Lysates/proteins at 10 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution
Predicted band size: 49, 50, 40 kDa
Observed band size: 83 kDa why is the actual band size different from the predicted?
Exposure time: 3 secondsThis data was developed using ab195207, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer: 5% NFDM/TBST.
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This data was developed using ab195207, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized RAW 264.7 (Mouse macrophage cells transformed with Abelson murine leukemia virus) cells labeling pan-myc with ab195207 at 1/250 dilution, followed by Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) secondary antibody at 1/1000 dilution (green).Confocal image showing nuclear staining on RAW 264.7 cell line.The nuclear counterstain is DAPI (blue).Tubulin is detected with ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution and ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/1000 dilution (red).The negative controls are as follows:--ve control 1: ab195207 at 1/250 dilution followed by ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/1000 dilution.-ve control 2: ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution followed by ab150077 (Alexa Fluor®488 Goat Anti-Rabbit IgG H&L) at 1/1000 dilution. -
All lanes : Anti-pan-myc antibody [EPR18863] (ab195207) at 1/1000 dilution
Lane 1 : HeLa (Human epithelial cells from cervix adenocarcinoma) whole cell lysate
Lane 2 : HEK-293 (Human epithelial cells from embryonic kidney) whole cell lysate
Lysates/proteins at 10 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution
Predicted band size: 49, 50, 40 kDa
Observed band size: 57 kDa why is the actual band size different from the predicted?
Exposure time: 3 minutesThis data was developed using ab195207, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer: 5% NFDM/TBST.
-
This data was developed using ab195207, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized HeLa (Human epithelial cells from cervix adenocarcinoma) cells labeling pan-myc with ab195207 at 1/250 dilution, followed by Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) secondary antibody at 1/1000 dilution (green).Confocal image showing nuclear staining on HeLa cell line.The nuclear counterstain is DAPI (blue).Tubulin is detected with ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution and ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/1000 dilution (red).The negative controls are as follows:--ve control 1: ab195207 at 1/250 dilution followed by ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/1000 dilution.-ve control 2: ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution followed by ab150077 (Alexa Fluor®488 Goat Anti-Rabbit IgG H&L) at 1/1000 dilution. -
This data was developed using ab195207, the same antibody clone in a different buffer formulation.Flow cytometry analysis of HeLa cells labelling pan-myc (red) with purified ab195207 at dilution of 1/60. The secondary antibody used was Alexa Fluor® 488 goat-anti-rabbit IgG (1/2000). Cells were fixed with 4% paraformaldehyde and permeabilised with 90% methanol. Isotype control antibody was Rabbit monoclonal IgG (black). The blue line shows cells without incubation with primary antibody and secondary antibody.
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All lanes : Anti-pan-myc antibody [EPR18863] (ab195207) at 1/1000 dilution
Lane 1 : HEK-293 (Human epithelial cells from embryonic kidney) whole cell lysate transfected with empty vector (vector control)
Lane 2 : HEK-293 whole cell lysate transfected with c-Myc
Lysates/proteins at 10 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution
Predicted band size: 49, 50, 40 kDa
Observed band size: 57 kDa why is the actual band size different from the predicted?
Exposure time: 3 minutesThis data was developed using ab195207, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer: 5% NFDM/TBST.
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All lanes : Anti-pan-myc antibody [EPR18863] (ab195207) at 1/2000 dilution
Lane 1 : HEK-293 (Human epithelial cells from embryonic kidney) whole cell lysate transfected with empty vector (vector control)
Lane 2 : HEK-293 whole cell lysate transfected with L-Myc with GFP-tag
Lysates/proteins at 10 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution
Predicted band size: 49, 50, 40 kDa
Observed band size: 83, 57 kDa why is the actual band size different from the predicted?
Exposure time: 3 minutesThis data was developed using ab195207, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer: 5% NFDM/TBST.
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Anti-pan-myc antibody [EPR18863] (ab195207) at 1/1000 dilution + RAW 264.7 (Mouse macrophage cells transformed with Abelson murine leukemia virus) whole cell lysate at 10 µg
Secondary
Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution
Predicted band size: 49, 50, 40 kDa
Observed band size: 60 kDa why is the actual band size different from the predicted?
Exposure time: 30 secondsThis data was developed using ab195207, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer: 5% NFDM/TBST.
The observed molecular weight for the mouse species is slightly higher than human Myc, this could be due to different degree of glycosylation.
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Anti-pan-myc antibody [EPR18863] (ab195207) at 1/2000 dilution + K562 (Human chronic myelogenous leukemia cells from bone marrow) whole cell lysate at 20 µg
Secondary
Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution
Predicted band size: 49, 50, 40 kDa
Observed band size: 57 kDa why is the actual band size different from the predicted?
Exposure time: 3 minutesThis data was developed using ab195207, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer: 5% NFDM/TBST.
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