Anti-BST2/Tetherin antibody [EPR20202-169]
- RabMAb
- Recombinant
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(4 Publications)
Rabbit Recombinant Monoclonal BST2/Tetherin antibody. Suitable for IP, Flow Cyt, WB, ICC/IF and reacts with Human samples. Cited in 4 publications.
View Alternative Names
CD317, Bone marrow stromal antigen 2, BST-2, HM1.24 antigen, Tetherin, BST2
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-BST2/Tetherin antibody [EPR20202-169] (AB243229)
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized U-937 (human histiocytic lymphoma cell line) cells labeling BST2/Tetherin with ab243229 at 1/100 dilution, followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) secondary antibody at 1/1000 dilution (Green). Confocal image showing cytoplasmic staining in U-937 cells (PMID : 20529266).
The nuclear counter stain is DAPI (blue). Tubulin is detected with Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) (ab195889) (red) at 1/200 dilution.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) secondary antibody at 1/1000 dilution.
- Flow Cyt
Unknown
Flow Cytometry - Anti-BST2/Tetherin antibody [EPR20202-169] (AB243229)
Flow cytometric analysis of HeLa (Human epithelial cell line from cervix adenocarcinoma) cell line labeling BST2/Tetherin with ab243229 at 1/500 dilution (Red) compared with a Rabbit IgG, monoclonal [EPR25A] - Isotype Control (ab172730) (black) and an unlabeled control (cells without incubation with primary antibody and secondary antibody) (blue). Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/2000 dilution was used as the secondary antibody. Gated on viable cells.
- Flow Cyt
Unknown
Flow Cytometry - Anti-BST2/Tetherin antibody [EPR20202-169] (AB243229)
Flow cytometric analysis of U-937 (human histiocytic lymphoma cell line) cell line labeling BST2/Tetherin with ab243229 at 1/500 dilution (red) compared with a Rabbit IgG, monoclonal [EPR25A] - Isotype Control (ab172730) (black) and an unlabeled control (cells without incubation with primary antibody and secondary antibody) (blue). Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/2000 dilution was used as the secondary antibody. Gated on viable cells.
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-BST2/Tetherin antibody [EPR20202-169] (AB243229)
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized HeLa (human epithelial cell line from cervix adenocarcinoma) cells labeling BST2/Tetherin with ab243229 at 1/100 dilution, followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) secondary antibody at 1/1000 dilution (Green). Confocal image showing cytoplasmic staining in HeLa cells (PMID : 20529266).
The nuclear counter stain is DAPI (blue). Tubulin is detected with Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) (ab195889) (red) at 1/200 dilution.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) secondary antibody at 1/1000 dilution.
- IP
Unknown
Immunoprecipitation - Anti-BST2/Tetherin antibody [EPR20202-169] (AB243229)
BST2/Tetherin was immunoprecipitated from 0.35 mg HeLa (human epithelial cell line from cervix adenocarcinoma) whole cell lysate with ab243229 at 1/30 dilution. Western blot was performed on the immunoprecipitate using ab243229 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP) (ab131366) was used for detection at 1/5000 dilution.
Lane 1 : HeLa whole cell lysate 10 μg (input).
Lane 2 : ab243229 IP in HeLa whole cell lysate.
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab243229 in HeLa whole cell lysate.
Blocking/Diluting buffer and concentration : 5% NFDM/TBST
Exposure time : 3 seconds.
All lanes:
Immunoprecipitation - Anti-BST2/Tetherin antibody [EPR20202-169] (ab243229)
Predicted band size: 20 kDa
false
- WB
Unknown
Western blot - Anti-BST2/Tetherin antibody [EPR20202-169] (AB243229)
Blocking/Diluting buffer and concentration : 5% NFDM/TBST
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID : 19196977; PMID : 19737401).
BST2/Tetherin is a glycosylated protein, its calculated MW is 20kDa, and the observed MW is 35 kDa, which is consistent to the literature.
Both 35 and 70-kDa bands were detected under the reducing condition, whereas under the non-reducing condition, only the 70-kDa band was detected.
All lanes:
Western blot - Anti-BST2/Tetherin antibody [EPR20202-169] (ab243229) at 1/1000 dilution
Lane 1:
HeLa (human epithelial cell line from cervix adenocarcinom), whole cell lysate, in the loading buffer containing DTT at 20 µg
Lane 2:
HeLa whole cell lysate in the loading buffer without DTT at 20 µg
Lane 3:
K562 (human chronic myelogenous leukemia lymphoblast), whole cell lysate, in the loading buffer containing DTT at 20 µg
Lane 4:
K562 whole cell lysate in the loading buffer without DTT at 20 µg
Secondary
All lanes:
Western 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
Predicted band size: 20 kDa
Observed band size: 35 kDa,70 kDa
false
Exposure time: 48s
- WB
Unknown
Western blot - Anti-BST2/Tetherin antibody [EPR20202-169] (AB243229)
Blocking/Diluting buffer and concentration : 5% NFDM/TBST.
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID : 19737401)
All lanes:
Western blot - Anti-BST2/Tetherin antibody [EPR20202-169] (ab243229) at 1/1000 dilution
All lanes:
U937 (human histiocytic lymphoma cell line) whole cell lysate at 20 µg
Secondary
All lanes:
Western 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
Predicted band size: 20 kDa
Observed band size: 35 kDa,70 kDa
false
Related conjugates and formulations (2)
-
Anti-BST2/Tetherin antibody [EPR20202-169] - BSA and Azide free
-
Anti-BST2/Tetherin antibody [EPR20202-169] - BSA and Azide free (Detector)
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
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Shipped at conditions
Appropriate short-term storage duration
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Aliquoting information
Storage information
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Target data
Publications (4)
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JCO precision oncology 9:e2500404 PubMed40749151
2025
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Genome medicine 16:148 PubMed39696540
2024
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Frontiers in immunology 12:669241 PubMed34025670
2021
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Cells 10: PubMed33800686
2021
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