Anti-Proteasome subunit beta type 2 antibody [MCP165]
| Name | Anti-Proteasome subunit beta type 2 antibody [MCP165] |
|---|---|
| Supplier | Abcam |
| Catalog | ab22650 |
| Prices | $370.00 |
| Sizes | 50 µl |
| Host | Mouse |
| Clonality | Monoclonal |
| Isotype | IgG1 |
| Clone | MCP165 |
| Applications | FC IHC-P WB |
| Species Reactivities | Mouse, Human |
| Antigen | Full length protein corresponding to Human Proteasome subunit beta type 2 |
| Description | Mouse Monoclonal |
| Gene | PSMB2 |
| Conjugate | Unconjugated |
| Supplier Page | Shop |
Product images
![Lane 1 : Protein Marker IVLanes 2 - 7 : Anti-Proteasome subunit beta type 2 antibody [MCP165] (ab22650) at 1/1000 dilutionLane 1 : Protein Marker IVLane 2 : Protein extract from ciliary body of diseased human donor at 2 µgLane 3 : Protein extract from ciliary body of normal human donor at 2 µgLane 4 : Protein extract from ciliary body of diseased human donor at 2 µgLane 5 : Protein extract from ciliary body of normal human donor at 2 µgLane 6 : Protein extract from ciliary body of diseased human donor at 2 µgLane 7 : Protein extract from ciliary body of normal human donor at 2 µgSecondaryLanes 2 - 7 : HRP conjugated goat anti mouse antibodyObserved band size : 27 kDa (why is the actual band size different from the predicted?)This image is courtesy of an Abreview submitted by Dr Matthias ZenkelSee Abreview](http://www.bioprodhub.com/system/product_images/ab_products/2/sub_4/17005_ab22650_2.jpg)
Lane 1 : Protein Marker IVLanes 2 - 7 : Anti-Proteasome subunit beta type 2 antibody [MCP165] (ab22650) at 1/1000 dilutionLane 1 : Protein Marker IVLane 2 : Protein extract from ciliary body of diseased human donor at 2 µgLane 3 : Protein extract from ciliary body of normal human donor at 2 µgLane 4 : Protein extract from ciliary body of diseased human donor at 2 µgLane 5 : Protein extract from ciliary body of normal human donor at 2 µgLane 6 : Protein extract from ciliary body of diseased human donor at 2 µgLane 7 : Protein extract from ciliary body of normal human donor at 2 µgSecondaryLanes 2 - 7 : HRP conjugated goat anti mouse antibodyObserved band size : 27 kDa (why is the actual band size different from the predicted?)This image is courtesy of an Abreview submitted by Dr Matthias ZenkelSee Abreview
IHC image of ab22650 staining in human normal lymphoid formalin fixed paraffin embedded tissue section, performed on a Leica BondTM system using the standard protocol F. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20 mins. The section was then incubated with ab22650, 1µg/ml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.
![Overlay histogram showing HeLa cells stained with ab22650 (red line). The cells were fixed with 80% methanol (5 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 (ab22650, 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.](http://www.bioprodhub.com/system/product_images/ab_products/2/sub_4/17007_Proteasome-subunit-beta-type-2-Primary-antibodies-ab22650-2.jpg)
Overlay histogram showing HeLa cells stained with ab22650 (red line). The cells were fixed with 80% methanol (5 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 (ab22650, 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.
Product References
Interferon-gamma induces immunoproteasomes and the presentation of MHC - Interferon-gamma induces immunoproteasomes and the presentation of MHC
Arellano-Garcia ME, Misuno K, Tran SD, Hu S. PLoS One. 2014 Aug 7;9(8):e102878.
Different expression levels of the TAP peptide transporter lead to recognition of - Different expression levels of the TAP peptide transporter lead to recognition of
Durgeau A, El Hage F, Vergnon I, Validire P, de Montpreville V, Besse B, Soria JC, van Hall T, Mami-Chouaib F. J Immunol. 2011 Dec 1;187(11):5532-9.