Anti-HIV1 p24 antibody [39/5.4A] (ab9071)
Key features and details
- Mouse monoclonal [39/5.4A] to HIV1 p24
- Suitable for: WB, Radioimmunoprecipitation, ELISA, ICC/IF, Sandwich ELISA
- Reacts with: Species independent
- Isotype: IgG1
Overview
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Product name
Anti-HIV1 p24 antibody [39/5.4A]
See all HIV1 p24 primary antibodies -
Description
Mouse monoclonal [39/5.4A] to HIV1 p24 -
Host species
Mouse -
Specificity
Human Immunodeficiency Virus Type 1(HIV 1) p24 protein. No detectable reaction has been observed with HIV-2 or SIV (Simian Immunodeficiency Virus) viral lysates by ELISA or Western blot. -
Tested applications
Suitable for: WB, Radioimmunoprecipitation, ELISA, ICC/IF, Sandwich ELISAmore details -
Species reactivity
Reacts with: Species independent -
Immunogen
Tissue, cells or virus corresponding to HIV1 p24. ab9071 raised by immunizing BALB/c mice with purified HIV-1 (Strain IIIB) lysate.
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General notes
ab9071 is used to detect HIV-1 core protein in virus infected cells, cell lysates, culture fluid, serum or plasma.
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Properties
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Form
Liquid -
Storage instructions
Shipped on Dry Ice. Upon delivery aliquot. Store at -20°C. Avoid freeze / thaw cycle. -
Storage buffer
pH: 7.2
Constituent: PBS -
Concentration information loading...
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Purity
Protein G purified -
Purification notes
Purified from serum-free culture supernatant. -
Primary antibody notes
The antibody is used to detect HIV 1 core protein in virus infected cells as well as in viral or infected cell lysates. Studies on core antigen synthesis and metabolism can be performed using Western blotting or radioimmunoprecipitation analysis. Useful as solid phase for capture of p24 in an antigen ELISA format. -
Clonality
Monoclonal -
Clone number
39/5.4A -
Isotype
IgG1 -
Research areas
Images
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Immunoblot analysis of viral proteins in HEK293-derived cells transiently transfected with the proviral plasmid, pNL4-3. EV or POM121C (614–987) cells were transfected with 1.0 μg of pNL4-3. The cells were harvested 48 h post-transfection and lysates were subjected to immnoblot analyses with anti-HIV-1 p24 (top panel; the upper arrow indicated precursor Gag [PrGag], the lower arrow indicated CA), anti-HA (middle panel) and anti-CYPA (bottom panel). One representative set of results from three independent experiments is shown.
Whole-cell lysates were prepared as follows: cells were washed twice with phosphate-buffered saline (PBS) (-), suspended in PBS(-) (500 μl per 1 × 107 cells) and mixed with an equal volume of 2 × sample buffer (4% sodium dodecyl sulfate, 125 mM Tris-HCl, pH 6.8, 10% 2-mercaptoethanol, 10% glycerol, and 0.002% bromphenol blue). Proteins were solubilized by heating for 5 min at 95°C. Samples were subjected to SDS-PAGE, transferred to PVDF membranes, and reacted with mouse monoclonal antibody to HIV-1 p24 (#ab9071, Abcam, Inc., Cambridge, MA), or rabbit polyclonal antibody to CYPA (#BML-SA296, Enzo Life Sciences, Inc., Farmingdale, NY). Membranes were then incubated with horseradish peroxidase-conjugated secondary antibody (#NA934 for anti-rabbit IgG, #NA931 for ant-mouse IgG, #NA933 for anti-human IgG, Amersham Biosciences, Piscataway, NJ), and proteins were visualized by Western Lightning Plus-ECL (PerkinElmer, Waltham, MA) or enhanced chemiluminescence (Pierce Biotechnology, Rockford, IL).
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All lanes : Anti-HIV1 p24 antibody [39/5.4A] (ab9071) at 1/2000 dilution
Lane 1 : Mock transfected 293T cells - cell lysate
Lane 2 : 293T cells transfected with HIV DNA - cell lysate
Secondary
All lanes : HRP conjugated goat anti-mouse IgG
Developed using the ECL technique.
Performed under reducing conditions.
Observed band size: 24,25,41,55 kDa why is the actual band size different from the predicted?
Exposure time: 5 minutes