Anti-Cytokeratin 7 antibody [EPR17079] - BSA and Azide free (ab251287)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rabbit monoclonal [EPR17079] to Cytokeratin 7 - BSA and Azide free
- Suitable for: WB, IP, IHC-P
- Reacts with: Mouse, Rat
Overview
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Product name
Anti-Cytokeratin 7 antibody [EPR17079] - BSA and Azide free
See all Cytokeratin 7 primary antibodies -
Description
Rabbit monoclonal [EPR17079] to Cytokeratin 7 - BSA and Azide free -
Host species
Rabbit -
Tested applications
Suitable for: WB, IP, IHC-Pmore details -
Species reactivity
Reacts with: Mouse, Rat -
Immunogen
Recombinant fragment. This information is proprietary to Abcam and/or its suppliers.
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General notes
Ab251287 is the carrier-free version of ab199718. 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
ab251287 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
EPR17079 -
Isotype
IgG -
Research areas
Images
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This data was developed using ab199718, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse lung tissue labeling Cytokeratin 7 with ab199718 at 1/1600 dilution followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution. Cytoplasm staining on mouse lung tissue is observed. Counter stained with Hematoxylin. Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution. Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. -
All lanes : Anti-Cytokeratin 7 antibody [EPR17079] (ab199718) at 1/20000 dilution
Lane 1 : Mouse lung tissue lysate
Lane 2 : Mouse bladder tissue lysate
Lysates/proteins at 10 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 51 kDa
Observed band size: 45,51 kDa why is the actual band size different from the predicted?
Exposure time: 15 secondsThis data was developed using ab199718, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer: 5% NFDM/TBST.
~45 kDa bands are supported by the literature and competitor's products, which may be an isoform. The observed MW is consistent with what has been described in the literature PMID: 16265353.
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Anti-Cytokeratin 7 antibody [EPR17079] (ab199718) at 1/20000 dilution + Mouse skin tissue lysate at 10 µg
Secondary
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 51 kDa
Observed band size: 45,51 kDa why is the actual band size different from the predicted?
Exposure time: 3 minutesThis data was developed using ab199718, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer: 5% NFDM/TBST.
~45 kDa bands are supported by the literature and competitor's products, which may be an isoform. The observed MW is consistent with what has been described in the literature PMID: 16265353.
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All lanes : Anti-Cytokeratin 7 antibody [EPR17079] (ab199718) at 1/4000 dilution
Lane 1 : Rat bladder tissue lysate
Lane 2 : Rat lung tissue lysate
Lysates/proteins at 10 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 51 kDa
Observed band size: 45,51 kDa why is the actual band size different from the predicted?
Exposure time: 15 secondsThis data was developed using ab199718, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer: 5% NFDM/TBST.
~45 kDa bands are supported by the literature and competitor's products, which may be an isoform. The observed MW is consistent with what has been described in the literature PMID: 16265353.
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This data was developed using ab199718, the same antibody clone in a different buffer formulation.Immunohistochemical analysis of paraffin-embedded Mouse colon tissue labeling Cytokeratin 7 with ab199718 at 1/1600 dilution followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution. Cytoplasm staining on mouse colon tissue is observed. Counter stained with Hematoxylin. Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution. Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
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This data was developed using ab199718, the same antibody clone in a different buffer formulation.
Cytokeratin 7 was immunoprecipitated from 1mg of Mouse skin whole cell extract with ab199718 at 1/30 dilution. Western blot was performed from the immunoprecipitate using ab199718 at 1/1000 dilution. Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG, was used as secondary antibody at 1/1500 dilution.
Lane 1: Mouse skin whole cell extract 10 µg (Input). Lane 2: ab199718 IP in Mouse skin whole cell extract. Lane 3: Rabbit monoclonal IgG (ab172730) instead of ab199718 in Mouse skin whole cell extract.
Blocking and dilution buffer: 5% NFDM/TBST.
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