Anti-CD33 antibody [WM53] - BSA and Azide free
- Recombinant
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(8 Publications)
Mouse Recombinant Monoclonal CD33 antibody. Carrier free. Suitable for Flow Cyt, ICC/IF and reacts with Human samples. Cited in 8 publications.
View Alternative Names
CD33, SIGLEC3, Myeloid cell surface antigen CD33, Sialic acid-binding Ig-like lectin 3, gp67, Siglec-3
- Flow Cyt
Supplier Data
Flow Cytometry - Anti-CD33 antibody [WM53] - BSA and Azide free (AB252263)
This data was developed using the same antibody clone in a different buffer formulation containing PBS and sodium azide (ab30371).
Flow cytometry staining of human whole blood with ab30371 (right) or mouse IgG1 and kappa; (ab170190) isotype (left). Red blood cells of 200 µL were lysed, then cells were incubated for 30 mins on ice in 1 x PBS containing 10 µg/mL human IgG and 10 % normal goat serum to block FC receptors and non-specific protein-protein interactions followed by antibody (ab30371) or mouse IgG1 & kappa; (ab170190) isotype for 30 min on ice. The secondary antibody Goat anti-mouse IgG H&L (Alexa Fluor 488, Pre-absorbed) (ab150119) was used at 1/2000 dilution for 30 min on ice. The cells were simultaneously stained with CD14.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-CD33 antibody [WM53] - BSA and Azide free (AB252263)
This data was developed using the same antibody clone in a different buffer formulation containing PBS and sodium azide (ab30371).
ab30371 staining CD33 in HL-60 cells. The cells were fixed with 4% paraformaldehyde (10min), permeabilized with 0.1%PBS-Tween for 5 minutes and then blocked with 1% BSA/10% normal goat serum/0.3M glycine in 0.1%PBS-Tween for 1h. The cells were then incubated overnight at +4°C with ab30371 at 10µg/ml and ab6046, Rabbit polyclonal to beta Tubulin - Loading Control, at 1/1000 dilution. Cells were then incubated with ab150117, Goat Anti-Mouse IgG H&L (Alexa Fluor® 488) at 1/1000 dilution (shown in green) and ab150080, Goat polyclonal Secondary Antibody to Rabbit IgG - H&L (Alexa Fluor® 594) at 1/1000 dilution (shown in pseudocolor red). Nuclear DNA was labelled with DAPI (shown in blue).
Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
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Reactivity data
Product details
ab252263 is the carrier-free version of ab30371.
Want a custom formulation?
This antibody clone is manufactured by Abcam. If you require a custom buffer formulation or conjugation for your experiments, please contact orders@abcam.com
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
Properties and storage information
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Target data
Publications (8)
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Journal of immunological methods 361:1-20 PubMed20655312
2010
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Unspecified reactive species
Journal of leukocyte biology 79:46-58 PubMed16380601
2005
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Unspecified reactive species
European heart journal 26:1196-204 PubMed15734770
2005
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Journal of immunology (Baltimore, Md. : 1950) 174:517-24 PubMed15611278
2004
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Blood 105:1256-64 PubMed15388576
2004
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Blood 99:546-54 PubMed11781237
2002
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Proceedings of the National Academy of Sciences of 98:5764-9 PubMed11320212
2001
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Unspecified reactive species
The American journal of pathology 158:1473-80 PubMed11290565
2001
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Unspecified application
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Unspecified reactive species
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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