Anti-SIX1 antibody [1229] - BSA and Azide free (ab255759)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Mouse monoclonal [1229] to SIX1 - BSA and Azide free
- Suitable for: WB, IHC-P, ICC/IF
- Reacts with: Human
Overview
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Product name
Anti-SIX1 antibody [1229] - BSA and Azide free
See all SIX1 primary antibodies -
Description
Mouse monoclonal [1229] to SIX1 - BSA and Azide free -
Host species
Mouse -
Tested applications
Suitable for: WB, IHC-P, ICC/IFmore details -
Species reactivity
Reacts with: Human -
Immunogen
Recombinant fragment. This information is proprietary to Abcam and/or its suppliers.
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Positive control
- WB: A-204 cell lysate. IHC-P: Human lung, prostatic hyperplasia and skeletal muscle tissue. ICC/IF: A-204 cells.
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General notes
This antibody clone is manufactured by Abcam. If you require a custom buffer formulation or conjugation for your experiments, please contact orders@abcam.com.
ab255759 is the carrier-free version of ab252224. This format is designed for use in antibody labeling, including fluorochromes, metal isotopes, oligonucleotides, enzymes.
Our carrier-free formats are supplied in a buffer free of BSA, sodium azide and glycerol for higher conjugation efficiency.
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.
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
1229 -
Isotype
IgG1 -
Research areas
Images
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All lanes : Anti-SIX1 antibody [1229] (ab252224) at 0.545 µg/ml
Lane 1 : A-204 (human muscle rhabdomyosarcoma) whole cell lysate
Lane 2 : Caco-2 (human colorectal adenocarcinoma epithelial cell) whole cell lysate
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Peroxidase-Conjugated Goat anti-Mouse IgG (H+L) at 1/5000 dilution
Predicted band size: 32 kDa
Exposure time: 3 minutesThis data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab252224).
Blocking/Dilution buffer: 5% NFDM/TBST.
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Formalin-fixed paraffin-embedded human lung tissue stained for SIX1 using ab252224 at 5.45µg/ml followed by a ready to use secondary antibody.
Nuclear staining on human lung tissue.
The section was incubated with ab252224 for 30 mins at room temperature.
The immunostaining staining was performed on a Leica Biosystems BOND® RX instrument.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab252224).
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4% Paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized A-204 (human muscle rhabdomyosarcoma) cells stained for SIX1 (Green) using ab252224 at 10.9µg/ml, followed by ab150077 AlexaFluor®488 Goat anti-Rabbit secondary antibody at 1/1000 dilution. ab195889 anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) was used as a counterstain at 1/200 dilution. Confocal image showing nuclear staining in A-204 cell line.
Negative control: Caco-2.This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab252224).
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Formalin-fixed paraffin-embedded human skeletal muscle tissue stained for SIX1 using ab252224 at 5.45µg/ml followed by a ready to use secondary antibody.
Nuclear staining on human skeletal muscle tissue.
The section was incubated with ab252224 for 30 mins at room temperature.
The immunostaining staining was performed on a Leica Biosystems BOND® RX instrument.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab252224).
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Formalin-fixed paraffin-embedded human prostatic hyperplasia tissue stained for SIX1 using ab252224 at 5.45µg/ml followed by a ready to use secondary antibody.
Nuclear staining on human prostatic hyperplasia.
The section was incubated with ab252224 for 30 mins at room temperature.
The immunostaining staining was performed on a Leica Biosystems BOND® RX instrument.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab252224).
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