Anti-Bassoon/BSN antibody [SAP7F407] (ab82958)
Key features and details
- Mouse monoclonal [SAP7F407] to Bassoon/BSN
- Suitable for: WB, ICC/IF, IHC-P
- Reacts with: Mouse, Rat, Human
- Isotype: IgG2a
Overview
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Product name
Anti-Bassoon/BSN antibody [SAP7F407]
See all Bassoon/BSN primary antibodies -
Description
Mouse monoclonal [SAP7F407] to Bassoon/BSN -
Host species
Mouse -
Tested Applications & Species
See all applications and species dataApplication Species ICC/IF RatIHC-P MouseRatHumanWB Rat -
Immunogen
Recombinant full length protein corresponding to Rat Bassoon/BSN.
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Positive control
- Rat brain tissue extract This antibody gave a positive result in IHC in the following FFPE tissue: Human normal cerebral cortex.
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General notes
This product was changed from ascites to tissue culture supernatant on 22nd May 2019. Please note that the dilutions may need to be adjusted accordingly. If you have any questions, please do not hesitate to contact our scientific support team.
This product was previously labelled as Bassoon
Properties
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Form
Liquid -
Storage instructions
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles. -
Storage buffer
Preservative: 0.09% Sodium azide
Constituents: 50% Glycerol, PBS -
Concentration information loading...
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Purity
Tissue culture supernatant -
Purification notes
Purified from TCS. -
Clonality
Monoclonal -
Clone number
SAP7F407 -
Isotype
IgG2a -
Research areas
Images
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Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Bassoon/BSN antibody [SAP7F407] (ab82958) This image is courtesy of an abreview submitted by Carl Hobbs, Kings's College London, United Kingdom.
IHC-P image of Bassoon/BSN staining on mouse cerebellum sections using ab82958 (1:1500). The sections were deparaffinized and subjected to heat mediated antigen retrieval using HEIR. The sections were blocked using 1% BSA for 10 mins at 21°C. ab82958 was diluted 1:1500 and incubated with the sctions for 2 hours at 21°C. The secondary antibody used was goat polyclonal to mouse IgG conjugated to Biotin (1:200).
This image was generated using the ascites version of the product.
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Anti-Bassoon/BSN antibody [SAP7F407] (ab82958) at 1/500 dilution + rat brain tissue extract
Developed using the ECL technique.
Predicted band size: 416 kDaThis image was generated using the ascites version of the product.
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Bassoon/BSN localization in the rat brain cerebellar molecular layer using Bassoon/BSN monoclonal antibody (ab82958).
This image was generated using the ascites version of the product.
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Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Bassoon/BSN antibody [SAP7F407] (ab82958) This image is courtesy of an abreview submitted by Carl Hobbs, Kings's College London, United Kingdom.
IHC-P image of Bassoon/BSN staining on rat cerebellum sections using ab82958 (1:1000). The sections were deparaffinized and subjected to heat mediated antigen retrieval using citric acid. The sections were blocked using 1% BSA for 10 mins at 21°C. ab82958 was diluted 1:1000 and incubated with the sections for 2 hours at 21°C. The secondary antibody used was goat polyclonal to mouse IgG conjugated to biotin (1:200).
This image was generated using the ascites version of the product.
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Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Bassoon/BSN antibody [SAP7F407] (ab82958)
IHC image of Bassoon/BSN staining in Human normal cerebral cortex formalin fixed paraffin embedded tissue section, performed on a Leica Bond™ 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 ab82958, 5µg/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.
This image was generated using the ascites version of the product.
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.