Anti-TAP2 antibody
3
(1 Review)
|
(7 Publications)
Rabbit Polyclonal TAP2 antibody. Suitable for WB, IHC-P, ICC/IF and reacts with Human samples. Cited in 7 publications. Immunogen corresponding to Recombinant Fragment Protein within Human TAP2 aa 400 to C-terminus.
View 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
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-TAP2 antibody (AB180611)
Immunocytochemistry/Immunofluorescence analysis of U2OS cells using ab180611. Blue DAPI for nuclear staining.
- WB
Lab
Western blot - Anti-TAP2 antibody (AB180611)
False colour image of Western blot : Anti-TAP2 antibody staining at 1/500 dilution, shown in green; Mouse anti-GAPDH antibody [6C5] (ab8245) loading control staining at 1/20000 dilution, shown in red. In Western blot, ab180611 was shown to bind specifically to TAP2. A band was observed at 75 kDa in wild-type HeLa cell lysates with no signal observed at this size in Tap2 knockout cell line ab265426 (knockout cell lysate ab258712). To generate this image, wild-type and Tap2 knockout HeLa cell lysates were analysed. First, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 3 % milk in TBS-0.1 % Tween® 20 (TBS-T) before incubation with primary antibodies overnight at 4 °C. Blots were washed four times in TBS-T, incubated with secondary antibodies for 1 h at room temperature, washed again four times then imaged. Secondary antibodies used were Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed (ab216776) at 1/20000 dilution.
All lanes:
Western blot - Anti-TAP2 antibody (ab180611) at 1/500 dilution
Lane 1:
Wild-type HeLa cell lysate at 20 µg
Lane 2:
Tap2 knockout HeLa cell lysate at 20 µg
Lane 2:
Western blot - Human TAP2 knockout HeLa cell line (<a href='/en-us/products/cell-lines/human-tap2-knockout-hela-cell-line-ab265426'>ab265426</a>)
Predicted band size: 76 kDa
Observed band size: 75 kDa
false
- WB
Lab
Western blot - Anti-TAP2 antibody (AB180611)
False colour image of Western blot : Anti-TAP2 antibody staining at 1/500 dilution, shown in green; Mouse anti-GAPDH antibody [6C5] (ab8245) loading control staining at 1/20000 dilution, shown in red. In Western blot, ab180611 was shown to bind specifically to TAP2. A band was observed at 70 kDa in treated wild-type A431 cell lysates with no signal observed at this size in Tap2 knockout cell line ab269617 (knockout cell lysate ab272427). To generate this image, wild-type and Tap2 knockout A431 cell lysates were analysed. First, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 3 % milk in TBS-0.1 % Tween® 20 (TBS-T) before incubation with primary antibodies overnight at 4 °C. Blots were washed four times in TBS-T, incubated with secondary antibodies for 1 h at room temperature, washed again four times then imaged. Secondary antibodies used were Goat anti-Rabbit IgG H&L 800CW and Goat anti-Mouse IgG H&L 680RD at 1/20000 dilution.
All lanes:
Western blot - Anti-TAP2 antibody (ab180611) at 1/500 dilution
Lane 1:
Wild-type A431 Treated IFNgamma (10 ng/mL, 16 h) cell lysate at 20 µg
Lane 2:
Tap2 knockout A431 Treated IFNgamma (10 ng/mL, 16 h) cell lysate at 20 µg
Lane 3:
Wild-type A431 Vehicle control IFNgamma (0 ng/mL, 16 h) cell lysate at 20 µg
Lane 4:
Tap2 knockout A431 Vehicle control IFNgamma (0 ng/mL, 16 h) cell lysate at 20 µg
Lane 5:
HeLa cell lysate at 20 µg
Secondary
Lanes 1 - 5:
Goat anti-Rabbit IgG H&L 800CW at 1/20000 dilution
Lanes 1 - 5:
Goat anti-Mouse IgG H&L 680RD at 1/20000 dilution
Observed band size: 70 kDa
false
- WB
Supplier Data
Western blot - Anti-TAP2 antibody (AB180611)
All lanes:
Western blot - Anti-TAP2 antibody (ab180611) at 1/500 dilution
All lanes:
Human placenta extract
Predicted band size: 76 kDa
false
Reactivity data
Properties and storage information
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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
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.
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Target data
Publications (7)
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Molecular cancer 24:80 PubMed40091029
2025
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Burns & trauma 12:tkad058 PubMed38250706
2024
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Frontiers in cellular and infection microbiology 12:979800 PubMed36619767
2022
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Scientific reports 11:9080 PubMed33907276
2021
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Cancer immunology research 5:1141-1151 PubMed29097421
2017
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Journal of immunology (Baltimore, Md. : 1950) 197:4807-4816 PubMed27821669
2016
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Journal of immunology (Baltimore, Md. : 1950) 196:4468-76 PubMed27183594
2016
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