Anti-Hsp27 antibody [8A7] (ab79868)
Key features and details
- Mouse monoclonal [8A7] to Hsp27
- Suitable for: Flow Cyt, IHC-P, ICC/IF, WB
- Reacts with: Mouse, Rat, Human
- Isotype: IgG1
Overview
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Product name
Anti-Hsp27 antibody [8A7]
See all Hsp27 primary antibodies -
Description
Mouse monoclonal [8A7] to Hsp27 -
Host species
Mouse -
Specificity
ab79868 recognizes Hsp25 and Hsp27, and cross reacts with alpha B crystallin. -
Tested Applications & Species
See all applications and species dataApplication Species Flow Cyt HumanICC/IF MouseIHC-P MouseHumanWB Rat -
Immunogen
Human Hsp27 peptide
Properties
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Form
Liquid -
Storage instructions
Shipped at 4°C. Store at -20°C. Stable for 12 months at -20°C. -
Storage buffer
Preservative: 0.09% Sodium azide
Constituents: PBS, 50% Glycerol -
Concentration information loading...
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Purity
Protein G purified -
Clonality
Monoclonal -
Clone number
8A7 -
Isotype
IgG1 -
Research areas
Images
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Immunohistochemistry analysis of Mouse backskin tissue using Mouse Anti-Hsp27 Monoclonal Antibody, at 1:100 dilution for 1 hour at RT. FITC Goat Anti-Mouse (green) was used as a Secondary Antibody at 1:50 dilutionfor 1 hour. Localization: Epidermis.
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Anti-Hsp27 antibody [8A7] (ab79868) at 1/1000 dilution + Rat lung tissue lysate
Predicted band size: 23 kDa
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ab79868 at 1/100,000 dilution staining Hsp27 in human colon cancer tissue section by Immunohistochemistry (Bouin's fixed paraffin-embedded tissue sections). Tissue underwent heat mediated antigen retrieval in microwave with two 5 minutes incubation intervals in citrate buffer. An antibody amplifier™ system was used for staining.
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ab79868 (1/100) staining Hsp27 in Mouse epidermis tissue sections by IF (Iimmunofluorescence). Secondary Antibody: FITC Goat Anti-Mouse (green) at 1:50 for 1 hour at RT.
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ab79868 staining Hsp27 in Mouse backskin tissue sections by ICC/IF (Immunocytochemistry/immunofluorescence).
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Overlay histogram showing HeLa cells stained with ab79868 (red line). The cells were fixed with 4% paraformaldehyde (10 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab79868, 1µg/1x106 cells) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22ºC. Isotype control antibody (black line) was mouse IgG1 [ICIGG1] (ab91353, 2µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed.