Anti-MHC class I antibody [OX18] - BSA and Azide free
- Recombinant
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(4 Publications)
Mouse Recombinant Monoclonal HLA A antibody. Carrier free. Suitable for Flow Cyt, IHC-Fr and reacts with Rat samples. Cited in 4 publications.
View Alternative Names
HLAA, HLA-A, Human leukocyte antigen A
- Flow Cyt
Supplier Data
Flow Cytometry - Anti-MHC class I antibody [OX18] - BSA and Azide free (AB244556)
This data was developed using the same antibody clone in a different buffer formulation (ab6405).
Lewis rat splenocytes stained with ab6405 (right) or mouse IgG1 kappa; (ab170190) isotype (left). Cells were incubated for 30 min on ice in 1x PBS containing 10 % rat serum to block FC receptors and non-specific protein-protein interaction followed by the antibody (ab6405) or mouse IgG1 kappa; (ab170190) isotype (1x 106 in 100 μL at 0.2 μg/mL) for 30 min on ice. The secondary antibody Goat anti-mouse IgG H&L (Alexa Fluor® 488, pre-adsorbed) (ab150117) was used at 1/2000 dilution for 30 min on ice. The cells were simultaneously stained with CD3. Acquisition of >30,000 events were collected using a 50 mW Blue laser (488nm) and 530/30 bandpass filter. Events were gated on live single cells.
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-MHC class I antibody [OX18] - BSA and Azide free (AB244556)
IHC image of MHC Class I staining in a section of frozen normal rat placenta*.
The section was fixed using 10% formaldehyde in 1XPBS for 10 minutes. No antigen retrieval step was performed prior to staining. Non-specific protein-protein interactions were then blocked in TBS containing 0.025% (v/v) Triton X-100, 0.3M glycine and 1% (w/v) BSA for 1h at room temperature. The section was then incubated overnight at +4°C in TBS containing 0.025% (v/v) Triton X-100 and 1% (w/v) BSA with ab6405 (shown in green) at 1 μg/ml. The section was then incubated with ab150117 (Goat polyclonal Secondary Antibody to Mouse IgG - H&L (Alexa Fluor® 488, 1/1000)) presabsorbed for 1 hour at room temperature. The secondary-only control image is taken from an identical assay without primary antibody. The section was then mounted using Fluoromount® .
Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
For IHC staining systems (automated and non-automated), customers should optimize variable parameters such as antibody concentrations and incubation times.
*Tissue obtained from Charles River.
This data was developed using the same antibody clone in a different buffer formulation containing PBS and sodium azide (ab6405).
Reactivity data
Product details
ab244556 is the carrier-free version of ab6405.
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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Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The molecules of MHC class I form part of the adaptive immune system. They act as a complex with peptides which are derived from proteins degraded by the proteasome. The peptide-MHC I complex travels to the cell surface where it engages with the T cell receptor (TCR) on cytotoxic T cells. This interaction is essential for immune surveillance ensuring the body identifies cells that might compromise health such as those infected by viruses or transformed malignantly.
Pathways
The function of MHC class I integrates into the antigen processing and presentation pathways. It is pivotal in the proteasome-dependent pathway for processing endogenous antigens. Proteins like TAP (transporter associated with antigen processing) assist in transporting peptides into the endoplasmic reticulum for loading onto MHC class I. This pathway is central to cellular immunity and intersects with various immune response cascades.
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Target data
Publications (4)
Recent publications for all applications. Explore the full list and refine your search
PloS one 10:e0135223 PubMed26263390
2015
Applications
Unspecified application
Species
Unspecified reactive species
ACS chemical neuroscience 2:676-683 PubMed22184511
2011
Applications
Unspecified application
Species
Unspecified reactive species
Blood 113:2079-87 PubMed19131548
2009
Applications
Unspecified application
Species
Unspecified reactive species
European journal of immunology 12:237-43 PubMed6178598
1982
Applications
Unspecified application
Species
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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