Anti-TAP1 antibody [EPR26236-92]
- BOND RX™ Validated
- Recombinant
- RabMAb
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Anti-TAP1 antibody [EPR26236-92] is a Rabbit Monoclonal antibody that is used in TAP1 Dot Blot, IHC-P, Western Blot. Suitable for Human samples.
Transporter associated with antigen processing 1 (TAP1) is a molecule involved in processing and presentation of major histocompatibility complex class I restricted antigens, including tumor-associated antigens. TAP1 participates in tumor immunity, and is aberrantly expressed in multiple cancer types, including in bladder cancer, small cell lung cancer, glioma, prostatic cancer, head and neck squamous cell carcinoma (HNSC), breast cancer, and colorectal cancer (CRC). Recently, TAP1 has been found to be a robust tumor prognostic biomarker and a novel predictor of clinical prognosis and immunotherapeutic responses in various cancer types
View Alternative Names
ABCB2, PSF1, RING4, Y3, TAP1, Antigen peptide transporter 1, APT1, ATP-binding cassette sub-family B member 2, Peptide supply factor 1, Peptide transporter PSF1, Peptide transporter TAP1, Peptide transporter involved in antigen processing 1, Really interesting new gene 4 protein, PSF-1
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TAP1 antibody [EPR26236-92] (AB322039)
Immunohistochemical analysis of paraffin-embedded Human colon tissue labeling TAP1 with ab322039 at 1/5000 (0.1 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining in human colon.
The section was incubated with ab322039 for 10 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Slides were incubated with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background
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-TAP1 antibody [EPR26236-92] (AB322039)
Immunohistochemical analysis of paraffin-embedded Human cervical carcinoma tissue labeling TAP1 with ab322039 at 1/5000 (0.1 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining in human cervical carcinoma.
The section was incubated with ab322039 for 10 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Slides were incubated with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background
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-TAP1 antibody [EPR26236-92] (AB322039)
Immunohistochemical analysis of paraffin-embedded (A) Untreated HT-29 (human colorectal adenocarcinoma epithelial cell). (B) HT-29 treated with IFN gamma (100 ng/mL) for 48 hours. tissue labeling TAP1 with ab322039 at 1/8000 (0.062 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Nearly no staining in (A) untreated HT-29, positive staining in (B) HT-29 treated with IFN gamma (100 ng/mL) for 48 hours.
The section was incubated with ab322039 for 10 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Slides were incubated with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background
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-TAP1 antibody [EPR26236-92] (AB322039)
Immunohistochemical analysis of paraffin-embedded Human skin tissue labeling TAP1 with ab322039 at 1/5000 (0.1 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining in human skin.
The section was incubated with ab322039 for 10 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Slides were incubated with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background
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-TAP1 antibody [EPR26236-92] (AB322039)
Immunohistochemical analysis of paraffin-embedded Human colon adenocarcinoma tissue labeling TAP1 with ab322039 at 1/5000 (0.1 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining in human colon carcinoma.
The section was incubated with ab322039 for 10 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Slides were incubated with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background
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
- WB
Supplier Data
Western blot - Anti-TAP1 antibody [EPR26236-92] (AB322039)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
The expression of TAP1 is upregulated in response to IFN gamma treatment.
The identity of the bands between 15 kDa and 40 kDa are unknown.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
All lanes:
Western blot - Anti-TAP1 antibody [EPR26236-92] (ab322039) at 1/1000 dilution
Lane 1:
Untreated HT-29 (human colorectal adenocarcinoma epithelial cell) whole cell lysate at 20 µg
Lane 2:
HT-29 treated with 100ng/ml IFN gamma for 48h whole cell lysate at 20 µg
Lane 3:
Untreated HeLa (human cervical adenocarcinoma epithelial cell) whole cell lysate at 20 µg
Lane 4:
HeLa treated with 100ng/ml IFN gamma for 48h whole cell lysate at 20 µg
Lane 5:
Human ovary cancer tissue lysate at 20 µg
Lane 6:
Human tonsil tissue lysate at 20 µg
Lane 7:
Human lung tissue lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 68 kDa,36 kDa
false
Exposure time: 1s
- Dot
Supplier Data
Dot Blot - Anti-TAP1 antibody [EPR26236-92] (AB322039)
Dot blot analysis of TAP1 using ab322039 at 1 : 1000 (0.498 ug/ml) followed by a Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1 : 100,000 dilution.
Lane1 : His-tagged human TAP1 fragment
Lane2 : His-tagged human TAP2 fragment
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
This antibody does not cross-react with human TAP2.
All lanes:
Dot Blot - Anti-TAP1 antibody [EPR26236-92] (ab322039) at 1/1000 dilution
Lane 1:
His-tagged human TAP1 fragment at 20 ng
Lane 2:
His-tagged human TAP2 fragment at 20 ng
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: 48s
Reactivity data
Product details
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.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
TAP1 participates in the immune system by facilitating the presentation of peptide antigens to T cells. It forms a complex with TAP2 to transport antigenic peptides necessary for the proper functioning of the MHC class I pathway. This complex is essential for the immune system's ability to detect and respond to pathogens. Proper functioning of TAP1 ensures that peptides presented on MHC class I molecules are of endogenous origin allowing T cells to monitor cellular health and detect infected or transformed cells.
Pathways
TAP1 plays a role in the antigen processing and presentation pathway which is critical for adaptive immunity. This pathway involves specific steps in peptide processing where TAP1 along with TAP2 is essential for translocating peptides for binding to MHC class I complexes. Other related proteins in this pathway include calreticulin and tapasin which assist in peptide loading onto MHC class I molecules. Additionally TAP1 is involved in regulating cytosolic proteins' turnover through its role in transporting peptides that result from degraded proteins.
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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'.
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