Anti-Cyclin A2 antibody [E23.1] - BSA and Azide free (ab264078)
![Anti-Cyclin A2 antibody [E23.1] - BSA and Azide free (ab264078)](https://www.abcam.com/ps/products/264/ab264078/Images/ab264078-355536-anti-cyclin-a2-antibody-e231-immunohistochemistry-tonsil-human.jpg "Anti-Cyclin A2 antibody [E23.1] - BSA and Azide free (ab264078)")
Key features and details
- Mouse monoclonal [E23.1] to Cyclin A2 - BSA and Azide free
- Suitable for: IHC-P, WB, IP, IHC-Fr
- Reacts with: Human
- Isotype: IgG2a
Overview
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Product name
Anti-Cyclin A2 antibody [E23.1] - BSA and Azide free
See all Cyclin A2 primary antibodies -
Description
Mouse monoclonal [E23.1] to Cyclin A2 - BSA and Azide free -
Host species
Mouse -
Tested applications
Suitable for: IHC-P, WB, IP, IHC-Frmore details -
Species reactivity
Reacts with: Human
Predicted to work with: Mouse, Rat, Chicken, Cow
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Immunogen
Fusion protein corresponding to Cow Cyclin A2.
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Positive control
- IHC-P: Human normal tonsil.
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General notes
Ab264078 is a PBS only version of ab38.
This antibody clone is manufactured by Abcam.
If you require this antibody in a particular buffer formulation or a particular conjugate for your experiments, please contact orders@abcam.com or you can find further information here.
Properties
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Form
Liquid -
Storage instructions
Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at +4°C. Do Not Freeze. -
Storage buffer
pH: 7.40
Constituent: PBS -
Carrier free
Yes -
Concentration information loading... -
Purity
Protein G purified -
Clonality
Monoclonal -
Clone number
E23.1 -
Myeloma
Sp2 -
Isotype
IgG2a -
Light chain type
kappa -
Research areas
Images
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Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Cyclin A2 antibody [E23.1] - BSA and Azide free (ab264078)
IHC image of Cyclin A staining in Human normal tonsil 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 ab38, 10µg/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.This data was developed using the same antibody clone in a different buffer formulation containing PBS and Sodium Azide (ab38)
