重组Anti-CD90 / Thy1抗体[EPR28145-53] - BSA and Azide free
Anti-CD90 / Thy1 antibody [EPR28145-53] - BSA and Azide free
- RabMAb
- Recombinant
- KO Validated
- 了解详情
Be the first to review this product! Submit a review
|
(0 Publication)
Knockout Tested Rabbit Recombinant Monoclonal CD90 / Thy1 antibody. Carrier free. Suitable for WB, ICC/IF, Flow Cyt, IP and reacts with Human, Mouse, Rat samples.
查看别名
CD90, Thy-1 membrane glycoprotein, CDw90, Thy-1 antigen, THY1
- Flow Cyt
Supplier Data
Flow Cytometry - Anti-CD90 / Thy1 antibody [EPR28145-53] - BSA and Azide free (AB307737)
This data was developed using ab307736, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of K-562 (human chronic myelogenous leukemia lymphoblast) (Left panel) compared to U-2 OS (human bone osteosarcoma epithelial cell) (Right panel) labeling CD90 / Thy1 with ab307736 at 1/500 dilution (0.1 µg) (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabeled control (cells without incubation with primary antibody and secondary antibody) (Blue). Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/2000 dilution was used as the secondary antibody.
Negative control : K-562.
Gated on viable cells.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-CD90 / Thy1 antibody [EPR28145-53] - BSA and Azide free (AB307737)
This data was developed using ab307736, the same antibody clone in a different buffer formulation. Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized U-2 OS (human bone osteosarcoma epithelial cell) cells labeling CD90 / Thy1 with ab307736 at 1/250 dilution (1.8 µg/ml) followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 dilution (2 µg/ml) (Green). Confocal image showing membranous and cytoplasmic staining in U-2 OS cell line, no staining was observed in K-562 cell line. Negative control : K-562 (PMID : 7683034). Image was taken with a confocal microscope(Leica-Microsystems, TCS SP8). ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 dilution (2.5 µg/ml) (Red). The nuclear counterstain was DAPI (Blue). Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution (2 µg/ml).
- IP
Supplier Data
Immunoprecipitation - Anti-CD90 / Thy1 antibody [EPR28145-53] - BSA and Azide free (AB307737)
This data was produced using ab307736 the same antibody clone but in a different buffer. CD90 / Thy1 was immunoprecipitated from 0.35 mg U-2 OS (human bone osteosarcoma epithelial cell) whole cell lysate 10 µg with ab307736 at 1/30 dilution (2 µg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab307736 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution. Lane 1 : U-2 OS whole cell lysate 10 µg Lane 2 : ab307736 IP in U-2 OS whole cell lysate Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab307736 in HU-2 OS whole cell lysate Blocking and dilution buffer and concentration : 5% NFDM/TBST. Exposure time : 15 seconds. The molecular weight observed is consistent with what has been described in the literature (PMID : 16770003) and due to the high glycosylation of the protein.
false
- IP
Supplier Data
Immunoprecipitation - Anti-CD90 / Thy1 antibody [EPR28145-53] - BSA and Azide free (AB307737)
This data was produced using ab307736 the same antibody clone but in a different buffer. CD90 / Thy1 was immunoprecipitated from 0.35 mg HuT-78 (human sezary syndrome cutaneous t lymphocyte) whole cell lysate 10 µg with ab307736 at 1/30 dilution (2 µg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab307736 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution. Lane 1 : HuT-78 whole cell lysate 10 µg Lane 2 : ab307736 IP in HuT-78 whole cell lysate Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab307736 in HuT-78 whole cell lysate Blocking and dilution buffer and concentration : 5% NFDM/TBST. Exposure time : 15 seconds. The molecular weight observed is consistent with what has been described in the literature (PMID : 16770003) and due to the high glycosylation of the protein.
false
- Flow Cyt
Supplier Data
Flow Cytometry - Anti-CD90 / Thy1 antibody [EPR28145-53] - BSA and Azide free (AB307737)
This data was developed using ab307736, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of Rabbit monoclonal IgG isotype control (ab172730) (Left panel) compared to mouse peripheral blood mononuclear cell (PBMC) (Right panel) labeling CD90 / Thy1 with ab307736 at 1/500 dilution (0.1 µg). Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/2000 dilution was used as the secondary antibody.
Cells were stained with rabbit IgG or ab307736 then stained with anti-CD3 conjugated to Alexa Fluor® 647.
Gated on viable cells.
- Flow Cyt
Supplier Data
Flow Cytometry - Anti-CD90 / Thy1 antibody [EPR28145-53] - BSA and Azide free (AB307737)
This data was developed using ab307736, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of PC-12 (rat adrenal gland pheochromocytoma) cells labeling CD90 / Thy1 with ab307736 at 1/500 dilution (0.1µg) (Red) compared with a Rabbit monoclonal IgG isotype control (ab172730) (Black) and an unlabeled control (cells without incubation with primary antibody and secondary antibody) (Blue). Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/2000 dilution was used as the secondary antibody. Gated on viable cells.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-CD90 / Thy1 antibody [EPR28145-53] - BSA and Azide free (AB307737)
This data was developed using ab307736, the same antibody clone in a different buffer formulation. Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized PC-12 (rat adrenal gland pheochromocytoma small irregularly shaped cells) cells labeling CD90 / Thy1 with ab307736 at 1/250 dilution (1.8 µg/ml) followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 dilution (2 µg/ml) (Green). Confocal image showing membranous and cytoplasmic staining in PC-12 cell line. Image was taken with a confocal microscope(Leica-Microsystems, TCS SP8). ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 dilution (2.5 µg/ml) (Red). The nuclear counterstain was DAPI (Blue). Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution (2 µg/ml).
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-CD90 / Thy1 antibody [EPR28145-53] - BSA and Azide free (AB307737)
This data was developed using ab307736, the same antibody clone in a different buffer formulation. Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized EL4 (mouse lymphoma T lymphocyte) cells labeling CD90 / Thy1 with ab307736 at 1/250 dilution (1.8 µg/ml) followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 dilution (2 µg/ml) (Green). Confocal image showing membranous and cytoplasmic staining in EL4 cell line. Image was taken with a confocal microscope(Leica-Microsystems, TCS SP8). ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 dilution (2.5 µg/ml) (Red). The nuclear counterstain was DAPI (Blue). Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution (2 µg/ml).
- WB
Lab
Western blot - Anti-CD90 / Thy1 antibody [EPR28145-53] - BSA and Azide free (AB307737)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab307736). Western blot : Anti-THY1 antibody [EPR28145-53] (ab307736) staining at 1/5000 dilution, shown in green; Mouse anti-Alpha Tubulin [DM1A] (ab7291) loading control staining at 1/20000 dilution, shown in red. In Western blot, ab307736 was shown to bind specifically to THY1. A band was observed at 25-37 kDa in wild-type U-2 OS cell lysates with no signal observed at this size in THY1 knockout cell line ab262490 (knockout cell lysate ab263925). To generate this image, wild-type and THY1 knockout U-2 OS 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-CD90 / Thy1 antibody [EPR28145-53] (<a href='/products/primary-antibodies/cd90-thy1-antibody-epr28145-53-ab307736'>ab307736</a>) at 1/5000 dilution
Lane 1:
Wild-type U-2 OS cell lysate at 30 µg
Lane 2:
Western blot - Human THY1 (CD90) knockout U-2 OS cell lysate (<a href='/products/cell-lysates/human-thy1-cd90-knockout-u-2-os-cell-lysate-ab263925'>ab263925</a>)
Lane 2:
Western blot - Human THY1 (CD90) knockout U-2 OS cell line (<a href='/products/cell-lines/human-thy1-cd90-knockout-u-2-os-cell-line-ab262490'>ab262490</a>)
Lane 2:
THY1 knockout U-2 OS cell lysate at 30 µg
Lane 3:
Human brain cell lysate at 2 µg
Lane 4:
Human kidney cell lysate at 20 µg
Lane 5:
K562 cell lysate at 30 µg
Secondary
All lanes:
Goat anti-Rabbit IgG H&L 800CW and Goat anti-Mouse IgG H&L 680RD at 1/20000 dilution
Predicted band size: 17 kDa
false
- WB
Supplier Data
Western blot - Anti-CD90 / Thy1 antibody [EPR28145-53] - BSA and Azide free (AB307737)
This data was developed using 307736, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : Negative control : K-562 (PMID : 7683034). The molecular weight observed is consistent with what has been described in the literature (PMID : 16770003). In Western blot, anti-GAPDH antibody (ab181602) loading control staining at 1/200, 000 dilution.This blot was developed using a high sensitivity ECL substrate Exposure time : 103 seconds
All lanes:
Western blot at 1/1000 dilution
Lane 1:
U-2 OS (human bone osteosarcoma epithelial cell) whole cell lysate
Lane 2:
K-562 (human chronic myelogenous leukemia lymphoblast) whole cell lysate
Lane 3:
EL4 (mouse lymphoma t lymphocyte) whole cell lysate
Secondary
All lanes:
Western blot at 1/2000 dilution
Observed band size: 25 kDa,37 kDa
false
Exposure time: 103s
- WB
Supplier Data
Western blot - Anti-CD90 / Thy1 antibody [EPR28145-53] - BSA and Azide free (AB307737)
This data was developed using 307736, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST. The molecular weight observed is consistent with what has been described in the literature (PMID : 16770003) and due to the highglycosylation of the protein. Exposure time : 48 seconds.
All lanes:
Western blot - Anti-CD90 / Thy1 antibody [EPR28145-53] (<a href='/products/primary-antibodies/cd90-thy1-antibody-epr28145-53-ab307736'>ab307736</a>) at 1/1000 dilution
Lane 1:
Human spleen tissue lysate at 20 µg
Lane 2:
HuT-78 (human sezary syndrome cutaneous t lymphocyte) whole cell lysate at 20 µg
Lane 3:
Mouse brain tissue lysate at 20 µg
Lane 4:
Rat brain tissue lysate at 20 µg
Lane 5:
PC-12 (rat adrenal gland pheochromocytoma cell) whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Observed band size: 25 kDa,37 kDa
false
Exposure time: 48s
不同偶联物与剂型 (5)
-
Anti-CD90 / Thy1 antibody [EPR28145-53]
-
519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-CD90 / Thy1 antibody [EPR28145-53]
-
617 Alexa Fluor® 594
Alexa Fluor® 594 Anti-CD90 / Thy1 antibody [EPR28145-53]
-
665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-CD90 / Thy1 antibody [EPR28145-53]
-
578 PE
PE Anti-CD90 / Thy1 antibody [EPR28145-53]
反应性数据
产品详情
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.
性能和储存信息
形式
纯化工艺
存储溶液
运输条件
推荐的短期储存条件
推荐的长期储存条件
补充信息
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
CD90 plays a role in cell-cell and cell-matrix interactions contributing to cellular adhesion migration and signal transduction. It functions as part of a complex involving integrins which mediate its interaction with the extracellular matrix. This protein also influences T-cell activation reflecting its importance in immune response regulation. Its presence aids in modulating response to injury and promoting tissue repair due to its association with stem and progenitor cells.
Pathways
CD90 engagement affects focal adhesion and MAPK signaling pathways. It interacts with integrins like αvβ3 and α5β1 influencing cell movement and proliferation processes. CD90 involvement in these pathways allows it to regulate responses important for cell survival and communication within various tissues. These interactions highlight the protein's role in maintaining cellular homeostasis and regulating physiological processes.
产品实验方案
- Visit the General protocols
- Visit the Troubleshooting
靶点信息
Abcam 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