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Rabbit Recombinant Monoclonal TAP2 antibody. Carrier free. Suitable for IP, Flow Cyt (Intra), ICC/IF, IHC-P, WB and reacts with Human samples.

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Images

Western blot - Anti-TAP2 antibody [EPR26237-82] - BSA and Azide free (AB307283), expandable thumbnail
  • Immunoprecipitation - Anti-TAP2 antibody [EPR26237-82] - BSA and Azide free (AB307283), expandable thumbnail
  • Immunohistochemistry - Anti-TAP2 antibody [EPR26237-82] - BSA and Azide free (AB307283), expandable thumbnail
  • Immunohistochemistry - Anti-TAP2 antibody [EPR26237-82] - BSA and Azide free (AB307283), expandable thumbnail
  • Immunohistochemistry - Anti-TAP2 antibody [EPR26237-82] - BSA and Azide free (AB307283), expandable thumbnail

Key facts

Isotype

IgG

Host species

Rabbit

Storage buffer

pH: 7.2 - 7.4
Constituents: 100% PBS

Form

Liquid

Clonality

Monoclonal

Immunogen

  • The exact immunogen used to generate this antibody is proprietary information.

Reactivity data

Select an application
Product promiseTestedExpectedPredictedNot recommended
IPFlow Cyt (Intra)ICC/IFIHC-PWB
Human
Tested
Tested
Tested
Tested
Tested
Mouse
Not recommended
Not recommended
Not recommended
Not recommended
Not recommended
Rat
Not recommended
Not recommended
Not recommended
Not recommended
Not recommended

Tested
Tested

Species

Human

Dilution info

-

Notes

-

Not recommended
Not recommended

Species

Rat, Mouse

Dilution info

-

Notes

-

Tested
Tested

Species

Human

Dilution info

-

Notes

-

Not recommended
Not recommended

Species

Rat, Mouse

Dilution info

-

Notes

-

Tested
Tested

Species

Human

Dilution info

-

Notes

-

Not recommended
Not recommended

Species

Rat, Mouse

Dilution info

-

Notes

-

Tested
Tested

Species

Human

Dilution info

-

Notes

Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.

Not recommended
Not recommended

Species

Rat

Dilution info

-

Notes

Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.

Species

Mouse

Dilution info

-

Notes

Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.

Tested
Tested

Species

Human

Dilution info

-

Notes

-

Not recommended
Not recommended

Species

Rat, Mouse

Dilution info

-

Notes

-

Target data

Function

ABC transporter associated with antigen processing. In complex with TAP1 mediates unidirectional translocation of peptide antigens from cytosol to endoplasmic reticulum (ER) for loading onto MHC class I (MHCI) molecules (PubMed:25377891, PubMed:25656091). Uses the chemical energy of ATP to export peptides against the concentration gradient (PubMed:25377891). During the transport cycle alternates between 'inward-facing' state with peptide binding site facing the cytosol to 'outward-facing' state with peptide binding site facing the ER lumen. Peptide antigen binding to ATP-loaded TAP1-TAP2 induces a switch to hydrolysis-competent 'outward-facing' conformation ready for peptide loading onto nascent MHCI molecules. Subsequently ATP hydrolysis resets the transporter to the 'inward facing' state for a new cycle (PubMed:11274390, PubMed:25377891, PubMed:25656091). Typically transports intracellular peptide antigens of 8 to 13 amino acids that arise from cytosolic proteolysis via IFNG-induced immunoproteasome. Binds peptides with free N- and C-termini, the first three and the C-terminal residues being critical. Preferentially selects peptides having a highly hydrophobic residue at position 3 and hydrophobic or charged residues at the C-terminal anchor. Proline at position 2 has the most destabilizing effect (PubMed:11274390, PubMed:7500034, PubMed:9256420). As a component of the peptide loading complex (PLC), acts as a molecular scaffold essential for peptide-MHCI assembly and antigen presentation (PubMed:1538751, PubMed:25377891, PubMed:26611325).

Alternative names

ABCB3, PSF2, RING11, Y1, TAP2, Antigen peptide transporter 2, APT2, ATP-binding cassette sub-family B member 3, Peptide supply factor 2, Peptide transporter PSF2, Peptide transporter TAP2, Peptide transporter involved in antigen processing 2, Really interesting new gene 11 protein, PSF-2, RING11

Recommended products

Rabbit Recombinant Monoclonal TAP2 antibody. Carrier free. Suitable for IP, Flow Cyt (Intra), ICC/IF, IHC-P, WB and reacts with Human samples.

Key facts

Isotype

IgG

Form

Liquid

Clonality

Monoclonal

Immunogen
  • The exact immunogen used to generate this antibody is proprietary information.
Carrier free

Yes

Clone number

EPR26237-82

Purification technique

Affinity purification Protein A

Concentration
Loading...

Storage

Shipped at conditions

Blue Ice

Appropriate short-term storage conditions

+4°C

Appropriate long-term storage conditions

+4°C

Notes

Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.

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.

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 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.

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.

Supplementary info

This supplementary information is collated from multiple sources and compiled automatically.

Activity summary

TAP2 also known as Transporter 2 ATP Binding Cassette Subfamily B Member has a mass of approximately 76 kDa. It functions as a part of the peptide-loading complex where it plays a mechanical role in transporting antigen peptides into the endoplasmic reticulum. TAP2 is expressed primarily in antigen-presenting cells such as B cells dendritic cells and macrophages. It is an integral membrane protein located in the membrane of the endoplasmic reticulum.

Biological function summary

The TAP2 protein operates as an important component of the immune system by facilitating the processing and presentation of antigens. It partners with TAP1 and forms a heterodimer complex essential for the transportation of peptides that are 8-16 amino acids long. This action is fundamental for the proper presentation of antigens on major histocompatibility complex (MHC) class I molecules which are pivotal in the recognition of infected or abnormal cells by cytotoxic T lymphocytes.

Pathways

The TAP2 protein plays a significant role in the antigen processing and presentation pathways. It directly impacts the MHC class I pathway by aiding in the selection and transport of peptides that bind to MHC class I molecules. TAP2 functions alongside related proteins such as TAP1 and tapasin which help facilitate the loading of these peptides onto MHC class I molecules in the endoplasmic reticulum preparing them for cell surface presentation.

Associated diseases and disorders

Mutations or deficiencies in the TAP2 gene are associated with bare lymphocyte syndrome type 1 (BLS1) a rare immunodeficiency disorder. This syndrome relates to a shortage of antigen presentation on MHC class I molecules leading to increased susceptibility to viral infections. TAP2 along with its partner protein TAP1 is critical in maintaining regular immune surveillance and any disruption in their function can result in profound immunological consequences including impaired cytotoxic T cell responses.

Product promise

We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.

In the unlikely event of one of our products not working as expected, you are covered by our product promise.

Full details and terms and conditions can be found here:
Terms & Conditions.

11 product images

  • Western blot - Anti-TAP2 antibody [EPR26237-82] - BSA and Azide free (ab307283), expandable thumbnail

    Western blot - Anti-TAP2 antibody [EPR26237-82] - BSA and Azide free (ab307283)

    This data was developed using Anti-TAP2 antibody [EPR26237-82] ab307282, the same antibody clone in a different buffer formulation.
    Samples are non-boiled as boiling may cause protein aggregates.

    The expression of TAP2 is upregulated in response to IFN gamma treatment (PMID: 1946428).

    Blocking/dilution buffer: 5% NFDM/TBST.

    Exposure time: 26 seconds.

    All lanes: Western blot - Anti-TAP2 antibody [EPR26237-82] (Anti-TAP2 antibody [EPR26237-82] ab307282) at 1/1000 dilution

    Lane 1: Wild-type HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate 20 μg

    Lane 2: TAP2 knockout HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate 20 μg

    Lane 3: Jurkat (human T cell leukemia T lymphocyte from peripheral blood) whole cell lysate 20 μg

    Lane 4: Raji (human Burkitts lymphoma B lymphocyte) whole cell lysate 20 μg

    Lane 5: Untreated HeLa (human epithelial cell line from cervix adenocarcinoma) whole cell lysate 20 μg

    Lane 6: HeLa treated with /ml IFN gamma for 16 hours whole cell lysate 20 μg

    Lane 7: MOLT-4 (human lymphoblastic leukemia T lymphoblast) whole cell lysate 20 μg

    Lane 8: HT-1080 (human fibrosarcoma epithelial cell) whole cell lysate 20 μg

    Lane 9: Human tonsil tissue lysate 20 μg

    Secondary

    All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/100000 dilution

    Observed band size: 75 kDa

    Exposure time: 26s

    Samples are non-boiled as boiling may cause protein aggregates.

    The expression of TAP2 is upregulated in response to IFN gamma treatment (PMID: 1946428).

    Blocking/dilution buffer: 5% NFDM/TBST.

    Exposure time: 26 seconds.

  • Immunoprecipitation - Anti-TAP2 antibody [EPR26237-82] - BSA and Azide free (ab307283), expandable thumbnail

    Immunoprecipitation - Anti-TAP2 antibody [EPR26237-82] - BSA and Azide free (ab307283)

    This data was developed using Anti-TAP2 antibody [EPR26237-82] ab307282, the same antibody clone in a different buffer formulation.
    TAP2 was immunoprecipitated from 0.35 mg HeLa (human epithelial cell line from cervix adenocarcinoma) treated with 10 ng/ml IFN gamma for 16 hours, whole cell lysate 10 ug with Anti-TAP2 antibody [EPR26237-82] ab307282 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using Anti-TAP2 antibody [EPR26237-82] ab307282 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(VeriBlot for IP Detection Reagent (HRP) ab131366) was used at 1/5000 dilution.

    Lane 1: HeLa treated with 10 ng/ml IFN gamma for 16 hours, whole cell lysate 10 ug

    Lane 2: Anti-TAP2 antibody [EPR26237-82] ab307282 IP in HeLa treated with 10 ng/ml IFN gamma for 16 hours, whole cell lysate

    Lane 3: Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of Anti-TAP2 antibody [EPR26237-82] ab307282 in HeLa treated with 10ng/ml IFN gamma for 16 hours, whole cell lysate

    Blocking and dilution buffer and concentration: 5% NFDM/TBST.

    Exposure time: 1 seconds.

    Input is non-boiled as boiling may cause protein aggregates.

    All lanes: Immunoprecipitation - Anti-TAP2 antibody [EPR26237-82] (Anti-TAP2 antibody [EPR26237-82] ab307282) at 1/1000 dilution

    Lane 1: HeLa (human epithelial cell line from cervix adenocarcinoma) treated with 10 ng/ml IFN gamma for 16 hours, whole cell lysate 10 μg

    Lane 2: HeLa treated with 10 ng/ml IFN gamma for 16 hours, whole cell lysate

    Lane 3: Immunoprecipitation - Rabbit IgG, monoclonal [EPR25A] - Isotype Control (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730)

    Secondary

    All lanes: Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (VeriBlot for IP Detection Reagent (HRP) ab131366) at 1/5000 dilution

    Observed band size: 75 kDa

    Exposure time: 1s

    TAP2 was immunoprecipitated from 0.35 mg HeLa (human epithelial cell line from cervix adenocarcinoma) treated with 10 ng/ml IFN gamma for 16 hours, whole cell lysate 10 ug with Anti-TAP2 antibody [EPR26237-82] ab307282 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using Anti-TAP2 antibody [EPR26237-82] ab307282 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(VeriBlot for IP Detection Reagent (HRP) ab131366) was used at 1/5000 dilution.

    Lane 1: HeLa treated with 10 ng/ml IFN gamma for 16 hours, whole cell lysate 10 ug

    Lane 2: Anti-TAP2 antibody [EPR26237-82] ab307282 IP in HeLa treated with 10 ng/ml IFN gamma for 16 hours, whole cell lysate

    Lane 3: Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of Anti-TAP2 antibody [EPR26237-82] ab307282 in HeLa treated with 10ng/ml IFN gamma for 16 hours, whole cell lysate

    Blocking and dilution buffer and concentration: 5% NFDM/TBST.

    Exposure time: 1 seconds.

    Input is non-boiled as boiling may cause protein aggregates.

  • Immunohistochemistry - Anti-TAP2 antibody [EPR26237-82] - BSA and Azide free (ab307283), expandable thumbnail

    Immunohistochemistry - Anti-TAP2 antibody [EPR26237-82] - BSA and Azide free (ab307283)

    This data was developed using Anti-TAP2 antibody [EPR26237-82] ab307282, the same antibody clone in a different buffer formulation.
    Immunohistochemical analysis of paraffin-embedded human liver tissue labeling TAP2 with Anti-TAP2 antibody [EPR26237-82] ab307282 at 1/2000 (0.257 ug/ml) followed by ready to use LeicaDS9800 (Bond® Polymer Refine Detection). Positive staining in human liver. The section was incubated with Anti-TAP2 antibody [EPR26237-82] ab307282 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 ready to use LeicaDS9800 (Bond® Polymer Refine Detection).

    Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.

  • Immunohistochemistry - Anti-TAP2 antibody [EPR26237-82] - BSA and Azide free (ab307283), expandable thumbnail

    Immunohistochemistry - Anti-TAP2 antibody [EPR26237-82] - BSA and Azide free (ab307283)

    This data was developed using Anti-TAP2 antibody [EPR26237-82] ab307282, the same antibody clone in a different buffer formulation.
    Immunohistochemical analysis of paraffin-embedded human breast tissue labeling TAP2 with Anti-TAP2 antibody [EPR26237-82] ab307282 at 1/2000 (0.257 ug/ml) followed by ready to use LeicaDS9800 (Bond® Polymer Refine Detection). Positive staining in human breast. The section was incubated with Anti-TAP2 antibody [EPR26237-82] ab307282 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 ready to use LeicaDS9800 (Bond® Polymer Refine Detection).

    Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.

  • Immunohistochemistry - Anti-TAP2 antibody [EPR26237-82] - BSA and Azide free (ab307283), expandable thumbnail

    Immunohistochemistry - Anti-TAP2 antibody [EPR26237-82] - BSA and Azide free (ab307283)

    This data was developed using Anti-TAP2 antibody [EPR26237-82] ab307282, the same antibody clone in a different buffer formulation.
    Immunohistochemical analysis of paraffin-embedded human tonsil tissue labeling TAP2 with Anti-TAP2 antibody [EPR26237-82] ab307282 at 1/2000 (0.257 ug/ml) followed by ready to use LeicaDS9800 (Bond® Polymer Refine Detection). Positive staining in human tonsil. The section was incubated with Anti-TAP2 antibody [EPR26237-82] ab307282 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 ready to use LeicaDS9800 (Bond® Polymer Refine Detection).

    Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.

  • Immunohistochemistry - Anti-TAP2 antibody [EPR26237-82] - BSA and Azide free (ab307283), expandable thumbnail

    Immunohistochemistry - Anti-TAP2 antibody [EPR26237-82] - BSA and Azide free (ab307283)

    This data was developed using Anti-TAP2 antibody [EPR26237-82] ab307282, the same antibody clone in a different buffer formulation.
    Immunohistochemical analysis of paraffin-embedded human breast cancer tissue labeling TAP2 with Anti-TAP2 antibody [EPR26237-82] ab307282 at 1/2000 (0.257 ug/ml) followed by ready to use LeicaDS9800 (Bond® Polymer Refine Detection). Positive staining in human breast cancer (PMID: 22065046). The section was incubated with Anti-TAP2 antibody [EPR26237-82] ab307282 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 ready to use LeicaDS9800 (Bond® Polymer Refine Detection).

    Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.

  • Immunohistochemistry - Anti-TAP2 antibody [EPR26237-82] - BSA and Azide free (ab307283), expandable thumbnail

    Immunohistochemistry - Anti-TAP2 antibody [EPR26237-82] - BSA and Azide free (ab307283)

    This data was developed using Anti-TAP2 antibody [EPR26237-82] ab307282, the same antibody clone in a different buffer formulation.
    Immunohistochemical analysis of paraffin-embedded Human cerebrum tissue labeling TAP2 with Anti-TAP2 antibody [EPR26237-82] ab307282 at 1/2000 (0.257 ug/ml) followed by a ready to use LeicaDS9800 (Bond? Polymer Refine Detection). Positive staining in human cerebrum. The section was incubated with Anti-TAP2 antibody [EPR26237-82] ab307282 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 with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins

  • Immunohistochemistry - Anti-TAP2 antibody [EPR26237-82] - BSA and Azide free (ab307283), expandable thumbnail

    Immunohistochemistry - Anti-TAP2 antibody [EPR26237-82] - BSA and Azide free (ab307283)

    This data was developed using Anti-TAP2 antibody [EPR26237-82] ab307282, the same antibody clone in a different buffer formulation.
    Immunohistochemical analysis of paraffin-embedded cell pellets labeling TAP2 with Anti-TAP2 antibody [EPR26237-82] ab307282 at 1/2000 (0.257 ug/ml) followed by ready to use LeicaDS9800 (Bond® Polymer Refine Detection).

    Positive staining in wild-type HeLa cell pellet and no staining in TAP2 knockout HeLa cell pellet.

    The section was incubated with Anti-TAP2 antibody [EPR26237-82] ab307282 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 ready to use LeicaDS9800 (Bond® Polymer Refine Detection).

    Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.

  • Immunocytochemistry/ Immunofluorescence - Anti-TAP2 antibody [EPR26237-82] - BSA and Azide free (ab307283), expandable thumbnail

    Immunocytochemistry/ Immunofluorescence - Anti-TAP2 antibody [EPR26237-82] - BSA and Azide free (ab307283)

    This data was developed using Anti-TAP2 antibody [EPR26237-82] ab307282, the same antibody clone in a different buffer formulation.
    Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized TAP2 KO HeLa (TAP2 knockout human cervical adenocarcinoma epithelial cell) ( Human TAP2 knockout HeLa cell line ab265426) cells labeling TAP2 with Anti-TAP2 antibody [EPR26237-82] ab307282 at 1/500 (1.028 ug/ml) dilution, followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 (2 ug/ml) dilution (Green).

    Confocal image showing endoplasmic reticulum staining in wildtype HeLa cells and no staining in TAP2 knockout HeLa cells.

    Image was taken with a confocal microscope(Leica-Microsystems, TCS SP8).

    ab12223 Anti-KDEL mouse monoclonal antibody was used to counterstain tubulin at 1/200 dilution (5 ug/ml) dilution, followed by Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed ab150120 Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) at a 1/1000 dilution (2 ug/ml) (Red). The nuclear counterstain was DAPI (Blue).

    Secondary antibody only control: Secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 ug/ml) dilution.

  • Immunohistochemistry - Anti-TAP2 antibody [EPR26237-82] - BSA and Azide free (ab307283), expandable thumbnail

    Immunohistochemistry - Anti-TAP2 antibody [EPR26237-82] - BSA and Azide free (ab307283)

    This data was developed using Anti-TAP2 antibody [EPR26237-82] ab307282, the same antibody clone in a different buffer formulation.
    Immunohistochemical analysis of paraffin-embedded human kidney tissue labeling TAP2 with Anti-TAP2 antibody [EPR26237-82] ab307282 at 1/2000 (0.257 ug/ml) followed by ready to use LeicaDS9800 (Bond® Polymer Refine Detection). Positive staining in human kidney. The section was incubated with Anti-TAP2 antibody [EPR26237-82] ab307282 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 ready to use LeicaDS9800 (Bond® Polymer Refine Detection).

    Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.

  • Flow Cytometry (Intracellular) - Anti-TAP2 antibody [EPR26237-82] - BSA and Azide free (ab307283), expandable thumbnail

    Flow Cytometry (Intracellular) - Anti-TAP2 antibody [EPR26237-82] - BSA and Azide free (ab307283)

    This data was developed using Anti-TAP2 antibody [EPR26237-82] ab307282, the same antibody clone in a different buffer formulation.
    Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized Wild-type HeLa (human cervix adenocarcinoma epithelial cell, Right) / TAP2 knockout HeLa (Left) cells labeling TAP2 with Anti-TAP2 antibody [EPR26237-82] ab307282 at 1/500 dilution (0.1ug) (Red) compared with a Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) (Black) isotype control and an unlabeled control (cells without incubation with primary antibody and secondary antibody) (Blue). A Goat Anti-Rabbit IgG (Alexa Fluor® 488, Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081) at 1/2000 dilution was used as the secondary antibody.

    Positive staining on HeLa cells (Human wild-type HeLa cell line ab255928), while no staining on TAP2 knockout HeLa cells (Human TAP2 knockout HeLa cell line ab265426).

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Product protocols

For this product, it's our understanding that no specific protocols are required. You can:

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