Anti-Trophoblast specific protein alpha antibody [EPR28905-557] - BSA and Azide free
- Advanced Validation
- BOND RX™ Validated
- Recombinant
- RabMAb
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Rabbit Recombinant Monoclonal Trophoblast specific protein alpha antibody. Carrier free. Suitable for Dot, IHC-P, mIHC and reacts with Recombinant fragment - Mouse, Mouse samples.
View Alternative Names
Tpbp, Tpbpa, Trophoblast-specific protein alpha
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Trophoblast specific protein alpha antibody [EPR28905-557] - BSA and Azide free (AB320824)
This data was developed using ab320823, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse spleen tissue labeling Trophoblast specific protein alpha with ab320823 at 1/1000 (0.516 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : No staining in mouse spleen.
The section was incubated with ab320823 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Trophoblast specific protein alpha antibody [EPR28905-557] - BSA and Azide free (AB320824)
This data was developed using ab320823, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse liver tissue labeling Trophoblast specific protein alpha with ab320823 at 1/1000 (0.516 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : No staining in mouse liver (PMID : 16251741).
The section was incubated with ab320823 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- mIHC
Lab
Multiplex immunohistochemistry - Anti-Trophoblast specific protein alpha antibody [EPR28905-557] - BSA and Azide free (AB320824)
This data was developed using ab320823, the same antibody clone in a different buffer formulation.
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded mouse placenta tissue staining LOX 1 with ab317689 at a 1/2000 dilution, ab324045 anti-AP2 gamma used at 1/500 dilution and ab320823 anti-Trophoblast specific protein alpha used at a 1/1000 dilution.
Panel A : merged staining of anti-LOX 1 (green; Opal™520), anti-AP2 gamma (magenta; Opal™690) and anti-Trophoblast specific protein alpha (gray; Opal™570) on mouse placenta.
Panel B : anti-LOX 1 staining trophoblast in mouse placenta.
Panel C : ant-AP2 gamma staining trophoblast stem cell in mouse placenta.
Panel D : ant-Trophoblast specific protein alpha staining junctional zone in mouse placenta.
Nuclear DNA was labeled with DAPI (shown in blue).
The section was incubated in three rounds of staining : in the order of ab317689, ab324045 and ab320823 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument with an Opal™ 4-color kit. Image acquisition was performed with Leica SP8 confocal microscope.
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Trophoblast specific protein alpha antibody [EPR28905-557] - BSA and Azide free (AB320824)
This data was developed using ab320823, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse placenta tissue labeling Trophoblast specific protein alpha with ab320823 at 1/1000 (0.516 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining in junctional zone of mouse placenta (PMID : 33884443).
The section was incubated with ab320823 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- Dot
Supplier Data
Dot Blot - Anti-Trophoblast specific protein alpha antibody [EPR28905-557] - BSA and Azide free (AB320824)
This data was developed using ab320823, the same antibody clone in a different buffer formulation.
Dot blot analysis of Trophoblast specific protein alpha using ab320823 at 1 : 1000 (0.516 ug/ml) followed by a Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1 : 100,000 dilution.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
All lanes:
Dot Blot - Anti-Trophoblast specific protein alpha antibody [EPR28905-557] (<a href='/en-us/products/primary-antibodies/trophoblast-specific-protein-alpha-antibody-epr28905-557-ab320823'>ab320823</a>) at 1/1000 dilution
All lanes:
His-tagged mouse Trophoblast specific protein alpha recombinant protein
Secondary
All lanes:
Dot Blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
false
Exposure time: 180s
Related conjugates and formulations (1)
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Anti-Trophoblast specific protein alpha antibody [EPR28905-557]
Reactivity data
Product details
ab320824 is the carrier-free version of ab320823.
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
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.
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
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Trophoblast associated protein ensures the successful interaction between the maternal and fetal interface. This protein is integral to the formation and maintenance of the maternal-fetal interface due to its adhesive properties. It forms part of a complex structure with other proteins involved in cellular adhesion processes which facilitate nutrient and gas exchange. The continued presence of trophoblast specific protein alpha is necessary for the structured and functional development of the fetal-maternal interface.
Pathways
Trophoblast glycoprotein participates in pathways essential for embryonic development and cellular adhesion. One major pathway is the Wnt signaling pathway where it interacts with cadherins to promote cell adhesion and tissue formation. Another pathway involves the MAPK/ERK pathway which influences trophoblast differentiation and survival with related proteins like N-cadherin playing a supporting role in the structural organization of the placenta.
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
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