Anti-Glycophorin A + B antibody [HIR2]
| Name | Anti-Glycophorin A + B antibody [HIR2] |
|---|---|
| Supplier | Abcam |
| Catalog | ab15009 |
| Prices | $391.00 |
| Sizes | 100 µg |
| Host | Mouse |
| Clonality | Monoclonal |
| Isotype | IgG2b |
| Clone | HIR2 |
| Applications | FC IHC-F IHC-P WB IP ICC/IF ICC/IF |
| Species Reactivities | Human |
| Antigen | Synthetic peptide corresponding to Human Glycophorin A + B (N terminal) |
| Description | Mouse Monoclonal |
| Gene | GYPA |
| Conjugate | Unconjugated |
| Supplier Page | Shop |
Product images
ab15009 staining Human normal lung tissue. Staining is localised to cellular membranes. Left panel: with primary antibody at 1 µg/ml. Right panel: isotype control. Sections were stained using an automated system DAKO Autostainer Plus, at RT. Sections were rehydrated and antigen retrieved with the Dako 3-in-1 antigen retrieval buffer citrate pH 6.0 in a DAKO PT Link. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 mins followed by blocking with Dako Protein block for 10 mins (containing casein 0.25% in PBS) then incubated with primary antibody for 20 mins and detected with Dako Envision Flex amplification kit for 30 mins. Colorimetric detection was completed with DAB for 5 mins. Slides were counterstained with Haematoxylin and coverslipped under DePeX. Please note that for manual staining we recommend to optimize the primary antibody concentration and incubation time (overnight incubation), and amplification may be required.
ICC/IF image of ab15009 staining of Glycophorin A + B in Human cord blood cells. The sections were incubated in 10% serum to block non-specific protein-protein interactions. The sections were then incubated with ab15009 (1:1000) for one hour at +24°C, followed by AlexaFluor®568 conjugated secondary antibody. Red staining of the human cord blood cell membrane was observed.See Abreview
![Overlay histogram showing K562 cells stained with ab15009 (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 (ab15009, 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 IgG2b [PLPV219] (ab91366, 2µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a positive signal in K562 cells fixed with 80% methanol (5 min)/permeabilized with 0.1% PBS-Tween for 20 min used under the same conditions.](http://www.bioprodhub.com/system/product_images/ab_products/2/sub_2/25813_ab15009-168657-untitled.png)
Overlay histogram showing K562 cells stained with ab15009 (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 (ab15009, 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 IgG2b [PLPV219] (ab91366, 2µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a positive signal in K562 cells fixed with 80% methanol (5 min)/permeabilized with 0.1% PBS-Tween for 20 min used under the same conditions.
Product References
Proteomic analysis of ERK1/2-mediated human sickle red blood cell membrane - Proteomic analysis of ERK1/2-mediated human sickle red blood cell membrane
Soderblom EJ, Thompson JW, Schwartz EA, Chiou E, Dubois LG, Moseley MA, Zennadi R. Clin Proteomics. 2013 Jan 3;10(1):1.
Terminal differentiation and loss of tumorigenicity of human cancers via - Terminal differentiation and loss of tumorigenicity of human cancers via
Zhang X, Cruz FD, Terry M, Remotti F, Matushansky I. Oncogene. 2013 May 2;32(18):2249-60, 2260.e1-21.
A novel fluorescence-based method in forensic science for the detection of blood - A novel fluorescence-based method in forensic science for the detection of blood
Thorogate R, Moreira JC, Jickells S, Miele MM, Daniel B. Forensic Sci Int Genet. 2008 Sep;2(4):363-71.
Flow cytometric analysis of human bone marrow perfusion cultures: erythroid - Flow cytometric analysis of human bone marrow perfusion cultures: erythroid
Rogers CE, Bradley MS, Palsson BO, Koller MR. Exp Hematol. 1996 Apr;24(5):597-604.
Cell surface antigen expression in human erythroid progenitors: erythroid and - Cell surface antigen expression in human erythroid progenitors: erythroid and
Nakahata T, Okumura N. Leuk Lymphoma. 1994 May;13(5-6):401-9.