Rabbit Recombinant Monoclonal M1 antibody. Carrier free. Suitable for IHC-P, ICC/IF, WB and reacts with Transfected cell line - Influenza A, Influenza A, Transfected cell lysate - Influenza A samples.
pH: 7.4
Constituents: 100% PBS
IHC-P | ICC/IF | WB | |
---|---|---|---|
Influenza A | Expected | Tested | Tested |
Transfected cell line - Influenza A | Tested | Not recommended | Not recommended |
Transfected cell lysate - Influenza A | Not recommended | Not recommended | Tested |
Species | Dilution info | Notes |
---|---|---|
Species Transfected cell line - Influenza A | Dilution info 1/1000 | Notes Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Influenza A | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Transfected cell lysate - Influenza A | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Influenza A | Dilution info 1/100 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Transfected cell line - Influenza A, Transfected cell lysate - Influenza A | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Transfected cell lysate - Influenza A | Dilution info 1/5000 | Notes - |
Species Influenza A | Dilution info 1/5000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Transfected cell line - Influenza A | Dilution info - | Notes - |
Matrix Protein 1, Matrix Protein I, Membrane matrix protein M1
Rabbit Recombinant Monoclonal M1 antibody. Carrier free. Suitable for IHC-P, ICC/IF, WB and reacts with Transfected cell line - Influenza A, Influenza A, Transfected cell lysate - Influenza A samples.
pH: 7.4
Constituents: 100% PBS
This product is a recombinant monoclonal antibody, which offers several advantages including:
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.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our 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.
For immunofluorescence analysis, Influenza A and B Virus infected cells slide were permeabilized for detection of Influenza A virus M1 matrix protein using ab308354 at 1/100 dilution (green).
Immunohistochemical analysis of Influenza A virus M1 transfected HEK293T cell pellet labeling Influenza A virus M1 matrix protein using ab308354 at 1/1000 dilution. Antigen retrival was performed using Citrate buffer, pH 6.0, 15 min
Non-transfected (–) and transfected (+) 293T whole cell extracts (30 μg) were separated by 12% SDS-PAGE, and the membrane was blotted with Influenza A virus M1 (matrix protein) antibody [HL1273] (ab308354) diluted at 1/5000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
All lanes: Western blot - Anti-Influenza A virus M1 matrix protein antibody [HL1273] (ab308354) at 1/5000 dilution
Lane 1: Non-transfected (–) 293T whole cell extracts at 30 µg
Lane 2: Transfected (+) 293T whole cell extracts at 30 µg
All lanes: HRP-conjugated anti-rabbit IgG antibody
Non-infected (–) and infected (+) H1299 whole cell extracts (15 μg) were separated by 12% SDS-PAGE, and the membrane was blotted with Influenza A virus M1 (matrix protein) antibody [HL1273] (ab308354) diluted at 1/5000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
All lanes: Western blot - Anti-Influenza A virus M1 matrix protein antibody [HL1273] (ab308354) at 1/5000 dilution
Lane 1: Non-infected (–) H1299 whole cell extracts at 15 µg
Lane 2: Infected (+) H1299 whole cell extracts at 15 µg
All lanes: HRP-conjugated anti-rabbit IgG antibody
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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