Anti-SIX1 antibody [1229] - BSA and Azide free
- BOND RX™ Validated
- Recombinant
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Mouse Recombinant Monoclonal SIX1 antibody. Carrier free. Suitable for WB, ICC/IF, IHC-P and reacts with Human samples.
View Alternative Names
Homeobox protein SIX1, Sine oculis homeobox homolog 1, SIX1
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-SIX1 antibody [1229] - BSA and Azide free (AB255759)
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).
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SIX1 antibody [1229] - BSA and Azide free (AB255759)
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).
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SIX1 antibody [1229] - BSA and Azide free (AB255759)
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).
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SIX1 antibody [1229] - BSA and Azide free (AB255759)
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).
- WB
Supplier Data
Western blot - Anti-SIX1 antibody [1229] - BSA and Azide free (AB255759)
This 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.
All lanes:
Western blot - Anti-SIX1 antibody [1229] (<a href='/en-us/products/primary-antibodies/six1-antibody-1229-ab252224'>ab252224</a>) at 0.545 µg/mL
Lane 1:
A-204 (human muscle rhabdomyosarcoma) whole cell lysate at 20 µg
Lane 2:
Caco-2 (human colorectal adenocarcinoma epithelial cell) whole cell lysate at 20 µg
Secondary
All lanes:
Peroxidase-Conjugated Goat anti-Mouse IgG (H+L) at 1/5000 dilution
Predicted band size: 32 kDa
true
Exposure time: 3min
Reactivity data
Product details
ab255759 is the carrier-free version of ab252224.
What are the advantages of a recombinant monoclonal antibody?
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 batch production
For more information, read more on recombinant antibodies.
Want a custom formulation?
This antibody clone is manufactured by Abcam. If you require a custom buffer formulation or conjugation for your experiments, please contact orders@abcam.com
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. 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 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
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.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
SIX1 influences cell proliferation survival and differentiation. As part of a transcriptional complex it interacts frequently with cofactors like EYA1 to execute its roles in developmental processes. These interactions allow SIX1 to impact gene targets that are important for tissue morphogenesis. The malfunctioning of these processes can lead to developmental disorders highlighting its role in the regulatory networks that govern organogenesis.
Pathways
Several essential biological processes involve SIX1 including the Wnt/β-catenin and TGF-β signaling pathways. In these pathways SIX1 sometimes regulates or interacts with proteins such as β-catenin enhancing transcriptional activation essential for cell fate determination. In the TGF-β pathway SIX1 influences epithelial-mesenchymal transition (EMT) an important event in embryogenesis and metastasis. These pathway involvements indicate its importance in maintaining cellular homeostasis and signaling balance.
Product protocols
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Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com