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Read our guarantee »Products:Immunology >> Adaptive Immunity >> MHC >> Class I
Anti-HLA Class I antibody [W6/32] - Azide free
See all HLA Class I products (12) ...
Mouse monoclonal [W6/32] to HLA Class I - Azide free
The antibody recognises an antigenic determinant common to HLA A, B and C. In WB, it detects the heavy chain of MHC molecule. We have data to indicate that this antibody may not cross react with Rabbit. However, this has not been conclusively tested and expression levels may vary in certain cell lines/tissues.
Flow Cyt, IP, WB, IHC-Fr, ELISA, ICC/IF, Functional Studiesmore details
Reacts with
Cow, Cat, Human
Tissue / cell preparation - Membrane of human tonsil cells.
Liquid
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze / thaw cycles.
Preservative: None
Constituents: PBS, pH 7.4
Concentration information loading...
Protein G purified
The antibody recognises virtually all nucleated human cells, it is a valuable reagent for analysing variations in HLA class I expression in different disease states e.g. liver disease, muscular dystrophy, inflammatory myopathy and other neuromuscular disorders. This antibody is also suitable as a positive control for HLA tissue typing and crossmatching.
Monoclonal
W6/32
IgG2a
Immunology >> Adaptive Immunity >> MHC >> Class I
Our Abpromise guarantee covers the use of ab23755 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Flow Cyt: Use 1µg for 106 cells. ((paraformaldehyde or methanol fixed cells))
IP: Use at an assay dependent dilution.
WB: 1/250 Use under non reducing condition. Detects a band of approximately 45 kDa (predicted molecular weight: 31 kDa).
IHC-Fr: Use at an assay dependent dilution.
ELISA: Use at an assay dependent dilution.
ICC/IF: Use a concentration of 1 µg/ml
FuncS: Use at an assay dependent dilution.
HLA CLass I is involved in the presentation of foreign antigens to the immune system.
Plasma membrane
Immunocytochemistry/ Immunofluorescence - HLA Class I antibody [W6/32] - Azide free (ab23755)
![Immunocytochemistry/ Immunofluorescence - HLA Class I antibody [W6/32] - Azide free (ab23755)](/ps/datasheet/images/23/ab23755/HLA-Class-I-Primary-antibodies-ab23755-1.jpg)
ICC/IF image of ab23755 stained HeLa cells. The cells were 4% formaldehyde fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab23755, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-mouse IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
Flow Cytometry - HLA Class I antibody [W6/32] - Azide free (ab23755)
![Flow Cytometry - HLA Class I antibody [W6/32] - Azide free (ab23755)](/ps/datasheet/images/23/ab23755/HLA-Class-I-Primary-antibodies-ab23755-2.jpg)
Overlay histogram showing Jurkat cells stained with ab23755 (red line). The cells were fixed with 4% paraformaldehyde (10 min) and incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab23755, 1µg/1x106 cells) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22°C. Isotype control antibody (black line) was mouse IgG2a [ICIGG2A] (ab91361, 2µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a positive signal in Jurkat cells fixed with methanol (5 min) used under the same conditions.
Please note that Abcam do not have data for use of this antibody on non-fixed cells. We welcome any customer feedback.
This product has been referenced in:
See all 4 publications for this product
Publishing research using ab23755? Please let us know so that we can cite the reference in this datasheet
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![Immunocytochemistry/ Immunofluorescence - HLA Class I antibody [W6/32] - Azide free (ab23755)](/ps/datasheet/images/23/ab23755/HLA-Class-I-Primary-antibodies-ab23755-1.jpg)
ICC/IF image of ab23755 stained HeLa cells. The cells were 4% formaldehyde fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab23755, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-mouse IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
![Flow Cytometry - HLA Class I antibody [W6/32] - Azide free (ab23755)](/ps/datasheet/images/23/ab23755/HLA-Class-I-Primary-antibodies-ab23755-2.jpg)
Overlay histogram showing Jurkat cells stained with ab23755 (red line). The cells were fixed with 4% paraformaldehyde (10 min) and incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab23755, 1µg/1x106 cells) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (
Please note that Abcam do not have data for use of this antibody on non-fixed cells. We welcome any customer feedback.
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