HRP Anti-Glutathione Peroxidase 4 antibody [EPNCIR144] (ab206266)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- HRP Rabbit monoclonal [EPNCIR144] to Glutathione Peroxidase 4
- Suitable for: WB
- Reacts with: Human
- Conjugation: HRP
Overview
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Product name
HRP Anti-Glutathione Peroxidase 4 antibody [EPNCIR144]
See all Glutathione Peroxidase 4 primary antibodies -
Description
HRP Rabbit monoclonal [EPNCIR144] to Glutathione Peroxidase 4 -
Host species
Rabbit -
Conjugation
HRP -
Tested Applications & Species
See all applications and species dataApplication Species WB Human -
Immunogen
Synthetic peptide. This information is proprietary to Abcam and/or its suppliers.
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Positive control
- WB: Human Testis and Fetal Liver tissue lysates; Jurkat and LNCaP whole cell lysates.
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General notes
This antibody was developed as part of a collaboration between Epitomics, the National Cancer Institute's Center for Cancer Research and the lab of Dolph Hatfield.
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 short term (1-2 weeks). Upon delivery aliquot. Store at -20°C. Avoid freeze / thaw cycle. Store In the Dark. -
Storage buffer
pH: 7.40
Preservative: 0.1% 10% Proclin 300 Solution
Constituents: 30% Glycerol (glycerin, glycerine), 1% BSA, PBS -
Concentration information loading...
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Purity
Protein A purified -
Clonality
Monoclonal -
Clone number
EPNCIR144 -
Isotype
IgG -
Research areas
Images
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All lanes : HRP Anti-Glutathione Peroxidase 4 antibody [EPNCIR144] (ab206266) at 1/5000 dilution
Lane 1 : Testis (Human) Tissue Lysate - adult normal tissue
Lane 2 : Liver (Human) Tissue Lysate - fetal normal tissue
Lane 3 : Jurkat (Human T cell lymphoblast-like cell line) Whole Cell Lysate
Lane 4 : LNCaP (Human prostate adenocarcinoma cell line) Whole Cell Lysate
Lysates/proteins at 10 µg per lane.
Developed using the ECL technique.
Performed under reducing conditions.
Predicted band size: 17 kDa
Observed band size: 20 kDa why is the actual band size different from the predicted?
Exposure time: 2 minutesThis blot was produced using a 4-12% Bis-tris gel under the MES buffer system. The gel was run at 200V for 35 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using 2% Bovine Serum Albumin before being incubated with ab206266 overnight at 4°C. Antibody binding was visualised using ECL development solution ab133406.
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