Anti-CD8 alpha antibody [RM1129] - BSA and Azide free
- BOND RX™ Validated
- Recombinant
- RabMAb
- 각 태그의 뜻
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Rabbit Recombinant Multiclonal CD8 alpha antibody. Carrier free. Suitable for WB, IP, IHC-P, ICC/IF, Flow Cyt, Flow Cyt (Intra) and reacts with Mouse, Human samples.
대체 명칭 보기
CD8a, MAL, CD8A, T-cell surface glycoprotein CD8 alpha chain, T-lymphocyte differentiation antigen T8/Leu-2
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-CD8 alpha antibody [RM1129] - BSA and Azide free (AB316779)
This data was developed using ab316778, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized Human PBMC (human peripheral blood mononuclear cell) cells labelling CD8 alpha with ab316778 at 1/500 dilution (0.1ug)/ Right (Red) compared with a Rabbit monoclonal IgG (ab172730) / Left isotype control.
Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody.
Cells are co-stianed with CD4 conjugated to Alexa Fluor®647.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD8 alpha antibody [RM1129] - BSA and Azide free (AB316779)
This data was developed using ab316778, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human colon tissue labeling CD8 alpha with ab316778 at 1/100 (4.95 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on T lymphocytes of human colon.
The section was incubated with ab316778 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 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-CD8 alpha antibody [RM1129] - BSA and Azide free (AB316779)
This data was developed using ab316778, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human tonsil tissue labeling CD8 alpha with ab316778 at 1/100 (4.95 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on human tonsil.
The section was incubated with ab316778 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 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-CD8 alpha antibody [RM1129] - BSA and Azide free (AB316779)
This data was developed using ab316778, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human gastric cancer tissue labeling CD8 alpha with ab316778 at 1/100 (4.95 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on T lymphocytes of human gastric cancer.
The section was incubated with ab316778 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 was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-CD8 alpha antibody [RM1129] - BSA and Azide free (AB316779)
This data was developed using ab316778, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized Human PBMC (human primary peripheral blood mononuclear cell) cells labellingCD8 alpha with ab316778 at 1/100 (4.95 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 (2 ug/ml) dilution.
Confocal image showing membranous and cytoplasmic staining in subsets of human PBMCs (shown in green). The counterstain was observed in red. Nuclear DNA was labeled with DAPI (shown in blue).
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 (2.5 ug/ml) dilution. The Nuclear counterstain was DAPI.
Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 ug/ml) dilution.
- IP
Supplier Data
Immunoprecipitation - Anti-CD8 alpha antibody [RM1129] - BSA and Azide free (AB316779)
This data was developed using ab316778, the same antibody clone in a different buffer formulation.
CD8 alpha was immunoprecipitated from 0.35 mg Human thymus tissue lysate with ab316778 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab316778 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : Human thymus tissue lysate
Lane 2 : ab316778 IP in Human thymus tissue lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab316778 in human thymus tissue lysate
All lanes:
Immunoprecipitation - Anti-CD8 alpha antibody [RM1129] (<a href='/ko/products/primary-antibodies/cd8-alpha-antibody-rm1129-ab316778'>ab316778</a>) at 1/30 dilution
All lanes:
Human thymus tissue lysate
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/ko/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
false
Exposure time: 93s
- Flow Cyt
Supplier Data
Flow Cytometry - Anti-CD8 alpha antibody [RM1129] - BSA and Azide free (AB316779)
This data was developed using ab316778, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of Mouse splenocytes cells labelling CD8 alpha with ab316778 at 1/50 dilution (1 ug)/Right compared with a Rabbit monoclonal IgG (ab172730) / Left isotype control.
Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody.
Gated on viable cells. Cells are co-stained with CD4 conjugated to Alexa Fluor®647.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CD8 alpha antibody [RM1129] - BSA and Azide free (AB316779)
This data was developed using ab316778, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse spleen tissue labeling CD8 alpha with ab316778 at 1/100 (4.95 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on mouse spleen.
The section was incubated with ab316778 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 was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-CD8 alpha antibody [RM1129] - BSA and Azide free (AB316779)
This data was developed using ab316778, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized Mouse splenocyte cells labellingCD8 alpha with ab316778 at 1/100 (4.95 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 (2 ug/ml) dilution.
Confocal image showing membranous and cytoplasmic staining in subsets of mouse splenocytes (shown in green). The counterstain was observed in red. Nuclear DNA was labeled with DAPI (shown in blue).
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 (2.5 ug/ml) dilution. The Nuclear counterstain was DAPI.
Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 ug/ml) dilution.
- IP
Supplier Data
Immunoprecipitation - Anti-CD8 alpha antibody [RM1129] - BSA and Azide free (AB316779)
This data was developed using ab316778, the same antibody clone in a different buffer formulation.
CD8 alpha was immunoprecipitated from 0.35 mg Mouse spleen tissue lysate with ab316778 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab316778 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : Mouse spleen tissue lysate
Lane 2 : ab316778 IP in Mouse spleen tissue lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab316778 in mouse spleen tissue lysate
All lanes:
Immunoprecipitation - Anti-CD8 alpha antibody [RM1129] (<a href='/ko/products/primary-antibodies/cd8-alpha-antibody-rm1129-ab316778'>ab316778</a>) at 1/30 dilution
All lanes:
Mouse spleen tissue lysate
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/ko/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
false
Exposure time: 6s
- WB
Supplier Data
Western blot - Anti-CD8 alpha antibody [RM1129] - BSA and Azide free (AB316779)
This data was developed using ab316778, the same antibody clone in a different buffer formulation.
Negative control : brain, heart and kidney.
The two bands are different isoforms that are consistent with the literature (PMID 3085089).
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
Exposure time : Lane 1-4 : 180 seconds Lane 5 : 10 seconds
All lanes:
Western blot - Anti-CD8 alpha antibody [RM1129] (<a href='/ko/products/primary-antibodies/cd8-alpha-antibody-rm1129-ab316778'>ab316778</a>) at 1/1000 dilution
Lane 1:
Mouse brain tissue lysate at 20 µg
Lane 2:
Mouse heart tissue lysate at 20 µg
Lane 3:
Mouse kidney tissue lysate at 20 µg
Lane 4:
Mouse spleen tissue lysate at 20 µg
Lane 5:
Mouse thymus tissue lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/ko/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 28-32 kDa,36 kDa
false
관련 conjugated 항체와 다양한 조성의 항체 (1)
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Anti-CD8 alpha antibody [RM1129]
Reactivity 정보
제품 세부 정보
ab316779 is the carrirer-free version of ab316778.
What are recombinant multiclonals?
Recombinant multiclonals are a mixture of recombinant antibodies co-expressed from a library of heavy and light chains. They offer several advantages including:
- - The sensitivity of polyclonal antibodies by recognising multiple epitopes
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
View our range of recombinant multiclonal antibodies.
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.
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.
특성 및 보관 정보
제형
Purification 테크닉
보관 버퍼
배송 시 보관 조건
적절한 단기 보관 조건
적절한 장기 보관 조건
추가 정보
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The CD8 alpha protein plays a critical role in T-cell mediated immune responses. It forms a heterodimer with the CD8 beta chain creating the CD8 alpha-beta complex that strengthens T-cell interaction with antigen-presenting cells. CD8 alpha also helps in signaling processes that activate T cells equipping them to destroy infected or malignant cells. Researchers often study CD8 alpha peptides to understand its interactions better.
Pathways
CD8 alpha is integral to the T-cell receptor signaling pathway and the cytotoxic T lymphocyte (CTL) pathway. The T-cell receptor complex which includes the CD8 molecule transmits signals that are important for T-cell activation and function. CD8 interacts with key proteins such as the T-cell receptor (TCR) and MHC class I molecules facilitating targeted responses against pathogens. These pathways highlight CD8 alpha’s role in adaptive immunity.
제품 프로토콜
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타겟 정보
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