Anti-CASK antibody [K56A/50] - BSA and Azide free (ab255764)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Mouse monoclonal [K56A/50] to CASK - BSA and Azide free
- Suitable for: IHC-P, WB
- Reacts with: Mouse, Rat, Human
Overview
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Product name
Anti-CASK antibody [K56A/50] - BSA and Azide free
See all CASK primary antibodies -
Description
Mouse monoclonal [K56A/50] to CASK - BSA and Azide free -
Host species
Mouse -
Tested applications
Suitable for: IHC-P, WBmore details
Unsuitable for: ICC/IF,IHC-Fr or IP -
Species reactivity
Reacts with: Mouse, Rat, Human -
Immunogen
Recombinant fragment. This information is proprietary to Abcam and/or its suppliers.
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Positive control
- WB: Human brain lysate; mouse brain lysate; rat brain lysate; mouse cerebellum lysate; rat cerebellum lysate. IHC-P: Rat liver, stomach and pancreas tissue; mouse liver tissue.
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General notes
ab255764 is the carrier-free version of ab252540.
This antibody clone is manufactured by Abcam. If you require a custom buffer formulation or conjugation for your experiments, please contact orders@abcam.com.
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. The carrier-free buffer and high concentration allow for increased conjugation efficiency.
This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free production
Properties
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Form
Liquid -
Storage instructions
Shipped at 4°C. Store at +4°C. Do Not Freeze. -
Storage buffer
pH: 7.2
Constituent: PBS -
Carrier free
Yes -
Concentration information loading...
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Purity
Protein A purified -
Clonality
Monoclonal -
Clone number
K56A/50 -
Isotype
IgG -
Research areas
Images
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All lanes : Anti-CASK antibody [K56A/50] (ab252540) at 1/1000 dilution
Lane 1 : Human brain tissue lysate
Lane 2 : Mouse brain tissue lysate
Lane 3 : Mouse cerebellum lysate
Lane 4 : Rat brain tissue lysate
Lane 5 : Rat cerebellum lysate
Lysates/proteins at 20 µg per lane.
Secondary
Lane 1 : Anti-mouse IgG for IP (HRP) (ab131368) at 1/100000 dilution
Lanes 2-5 : Peroxidase-Conjugated Goat anti-Mouse IgG(H+L) at 1/100000 dilution
Predicted band size: 105 kDa
Observed band size: 120 kDa why is the actual band size different from the predicted?Blocking and dilution buffer: 5% NFDM/TBST.
Exposure times.
Lane 1: 125 seconds; Lanes 2-5: 26 seconds.
The molecular weight observed is consistent with what has been described in the literature (PMID: 15236336).
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol and azide (ab252540).
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Immunohistochemical analysis of paraffin-embedded rat stomach tissue labeling CASK with ab252540 at 0.134µg/ml, followed by Goat Anti-Mouse IgG H&L (HRP polymer) (ab214879) ready to use. Membranous and cytoplasmic staining on rat stomach is observed. Counter stained with hematoxylin.
Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is Goat Anti-Mouse IgG H&L (HRP polymer) (ab214879) ready to use.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins.
The section was incubated with ab252540 for 30 mins at 37℃. The immunostaining staining was performed on a Leica Biosystems BOND® RX instrument.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol and azide (ab252540).
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Immunohistochemical analysis of paraffin-embedded rat pancreas tissue labeling CASK with ab252540 at 0.134µg/ml, followed by Goat Anti-Mouse IgG H&L (HRP polymer) (ab214879) ready to use. Membranous staining on rat pancreas is observed. Counter stained with hematoxylin.
Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is Goat Anti-Mouse IgG H&L (HRP polymer) (ab214879) ready to use.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins.
The section was incubated with ab252540 for 30 mins at 37℃. The immunostaining staining was performed on a Leica Biosystems BOND® RX instrument.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol and azide (ab252540).
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Immunohistochemical analysis of paraffin-embedded rat liver tissue labeling CASK with ab252540 at 0.134µg/ml, followed by Goat Anti-Mouse IgG H&L (HRP polymer) (ab214879) ready to use. Membranous staining on rat liver is observed. Counter stained with hematoxylin.
Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is Goat Anti-Mouse IgG H&L (HRP polymer) (ab214879) ready to use.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins.
The section was incubated with ab252540 for 30 mins at 37℃. The immunostaining staining was performed on a Leica Biosystems BOND® RX instrument.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol and azide (ab252540).
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Immunohistochemical analysis of paraffin-embedded mouse liver tissue labeling CASK with ab252540 at 0.134µg/ml, followed by Goat Anti-Mouse IgG H&L (HRP polymer) (ab214879) ready to use. Membranous staining on mouse liver is observed. Counter stained with hematoxylin.
Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is Goat Anti-Mouse IgG H&L (HRP polymer) (ab214879) ready to use.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins.
The section was incubated with ab252540 for 30 mins at 37℃. The immunostaining staining was performed on a Leica Biosystems BOND® RX instrument.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol and azide (ab252540).
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