Anti-Calmodulin 1/2/3 antibody [2D1]
1
(1 리뷰)
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(18 제품이 사용된 논문 )
Mouse Monoclonal CALM1 antibody. Suitable for Flow Cyt, IHC-P, WB, ELISA, IP, ICC/IF and reacts with Human, Rat, Dictyostelium discoideum, Mouse, Chicken, Cow samples. Cited in 18 publications.
대체 명칭 보기
CALM, CAM, CAM1, CALM1, Calmodulin-1, CALML2, CAM3, CAMC, CAMIII, CALM3, Calmodulin-3, CAM2, CAMB, CALM2, Calmodulin-2
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-Calmodulin 1/2/3 antibody [2D1] (AB2860)
Immunofluorescent analysis of HeLa (Human epithelial cell line from cervix adenocarcinoma) cells labeling Calmodulin with ab2860. Calmodulin staining (green) F-Actin staining with Phalloidin (red) and nuclei with DAPI (blue) is shown. Cells were grown on chamber slides and fixed with formaldehyde prior to staining. Cells were probed without (control) or with or an antibody recognizing Calmodulin ab2860 at a dilution of 1 : 50 over night at 4 °C washed with PBS and incubated with a DyLight-488 conjugated secondary antibody. Images were taken at 60X magnification.
- Flow Cyt
Lab
Flow Cytometry - Anti-Calmodulin 1/2/3 antibody [2D1] (AB2860)
Overlay histogram showing HeLa cells stained with ab2860 (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. The cells were then incubated with the antibody (ab2860, 2μg/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 IgG1 [ICIGG1] (ab91353, 2μg/1x106 cells ) used under the same conditions. Acquisition of >5,000 events was performed.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-Calmodulin 1/2/3 antibody [2D1] (AB2860)
Immunofluorescent analysis of A2058 (Human metastatic melanoma cell line) cells labeling Calmodulin ab2860. Calmodulin staining (green) F-Actin staining with Phalloidin (red) and nuclei with DAPI (blue) is shown. Cells were grown on chamber slides and fixed with formaldehyde prior to staining. Cells were probed without (control) or with or an antibody recognizing Calmodulin ab2860 at a dilution of 1 : 50 over night at 4 °C washed with PBS and incubated with a DyLight-488 conjugated secondary antibody. Images were taken at 60X magnification.
- Flow Cyt
Supplier Data
Flow Cytometry - Anti-Calmodulin 1/2/3 antibody [2D1] (AB2860)
Flow cytometry analysis of Calmodulin showing positive staining in the cytoplasm of MCF7 (Human breast adenocarcinoma cell line) cells compared to an isotype control (blue). Cells were harvested and adjusted to a concentration of 1-5x10^6 cells/ml. Cells were then fixed with 2% paraformaldehyde and washed with PBS. Cells were penetrated by dropping the supernatant and adding 90% methanol followed by incubation for 10 minutes at room temperature. Cells were blocked with a 2% solution of BSA-PBS for 30 min at room temperature and incubated with ab2860 at a dilution of 2 ug/test for 60 min at room temperature. Cells were then incubated for 40 min at room temperature in the dark using a Dylight 488-conjugated goat anti-mouse IgG (H+L) secondary antibody and re-suspended in PBS for FACS analysis.
- Flow Cyt
Unknown
Flow Cytometry - Anti-Calmodulin 1/2/3 antibody [2D1] (AB2860)
Flow cytometry analysis of Calmodulin showing positive staining in the cytoplasm of PC-12 (Rat adrenal gland pheochromocytoma cell line) cells compared to an isotype control (blue). Cells were harvested and adjusted to a concentration of 1-5x10^6 cells/ml. Cells were then fixed with 2% paraformaldehyde and washed with PBS. Cells were penetrated by dropping the supernatant and adding 90% methanol followed by incubation for 10 minutes at room temperature. Cells were blocked with a 2% solution of BSA-PBS for 30 min at room temperature and incubated with ab2860 at 2 ug/test for 60 min at room temperature. Cells were then incubated for 40 min at room temperature in the dark using a Dylight 488-conjugated goat anti-mouse IgG (H+L) secondary antibody and re-suspended in PBS for FACS analysis.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-Calmodulin 1/2/3 antibody [2D1] (AB2860)
Immunofluorescent analysis of C6 (Rat glial tumor cell line) cells labeling Calmodulin ab2860. Calmodulin staining (green) F-Actin staining with Phalloidin (red) and nuclei with DAPI (blue) is shown. Cells were grown on chamber slides and fixed with formaldehyde prior to staining. Cells were probed without (control) or with or an antibody recognizing Calmodulin ab2860 at a dilution of 1 : 50 over night at 4 °C washed with PBS and incubated with a DyLight-488 conjugated secondary antibody. Images were taken at 60X magnification.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Calmodulin 1/2/3 antibody [2D1] (AB2860)
Immunohistochemistry was performed on normal biopsies of deparaffinized rat cerebellum tissue. To expose target proteins heat induced antigen retrieval was performed using 10mM sodium citrate (pH6.0) buffer microwaved for 8-15 minutes. Following antigen retrieval tissues were blocked in 3% BSA-PBS for 30 minutes at room temperature. Tissues were then probed at a dilution of 1 : 20 with a mouse monoclonal antibody recognizing Calmodulin ab2860 or without primary antibody (negative control) overnight at 4°C in a humidified chamber. Tissues were washed extensively with PBST and endogenous peroxidase activity was quenched with a peroxidase suppressor. Detection was performed using a biotin-conjugated secondary antibody and SA-HRP followed by colorimetric detection using DAB. Tissues were counterstained with hematoxylin and prepped for mounting.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Calmodulin 1/2/3 antibody [2D1] (AB2860)
Immunohistochemistry was performed on normal biopsies of deparaffinized rat testis tissue. To expose target proteins heat induced antigen retrieval was performed using 10mM sodium citrate (pH6.0) buffer microwaved for 8-15 minutes. Following antigen retrieval tissues were blocked in 3% BSA-PBS for 30 minutes at room temperature. Tissues were then probed at a dilution of 1 : 20 with a mouse monoclonal antibody recognizing Calmodulin ab2860 or without primary antibody (negative control) overnight at 4°C in a humidified chamber. Tissues were washed extensively with PBST and endogenous peroxidase activity was quenched with a peroxidase suppressor. Detection was performed using a biotin-conjugated secondary antibody and SA-HRP followed by colorimetric detection using DAB. Tissues were counterstained with hematoxylin and prepped for mounting.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Calmodulin 1/2/3 antibody [2D1] (AB2860)
Immunolocalization of calmodulin in rat brain cells using ab2860 (1 : 100)
- Flow Cyt
Supplier Data
Flow Cytometry - Anti-Calmodulin 1/2/3 antibody [2D1] (AB2860)
Flow cytometry analysis of Calmodulin showing positive staining in the cytoplasm of C6 (Rat glial tumor cell line) cells compared to an isotype control (blue). Cells were harvested and adjusted to a concentration of 1-5x10^6 cells/ml. Cells were then fixed with 2% paraformaldehyde and washed with PBS. Cells were penetrated by dropping the supernatant and adding 90% methanol followed by incubation for 10 minutes at room temperature. Cells were blocked with a 2% solution of BSA-PBS for 30 min at room temperature and incubated with ab2860 at 2 ug/test for 60 min at room temperature. Cells were then incubated for 40 min at room temperature in the dark using a Dylight 488-conjugated goat anti-mouse IgG (H+L) secondary antibody and re-suspended in PBS for FACS analysis.
Reactivity 정보
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This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Calmodulin modulates intracellular activities by binding to calcium ions and interacting with a wide array of target proteins. It is not part of a molecular complex but can partner with proteins like kinases and phosphatases leading to downstream effects on diverse cellular processes. Calmodulin function extends to muscle contraction cell division and signal transduction impacting both basal and specialized cellular functions.
Pathways
Calmodulin operates as a functional link in calcium signaling and the MAPK signaling pathways. In these pathways calmodulin influences the activity of proteins such as myosin light-chain kinase and calmodulin-dependent protein kinase. These interactions showcase calmodulin's pivotal role in translating calcium signaling into cellular responses connecting several signaling cascades.
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제품이 사용된 논문 (18)
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NPJ science of food 9:178 PubMed40826004
2025
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Glia 73:2057-2076 PubMed40631759
2025
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Cell death & disease 15:429 PubMed38890273
2024
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iScience 27:109156 PubMed38439960
2024
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EMBO molecular medicine 14:e16501 PubMed36321563
2022
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Cells 11: PubMed35456008
2022
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International journal of molecular sciences 23: PubMed35269623
2022
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Heliyon 7:e07503 PubMed34401557
2021
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Scientific reports 9:12876 PubMed31578341
2019
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Antioxidants & redox signaling 30:542-559 PubMed29486586
2018
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