Rabbit Recombinant Monoclonal C1S antibody. Carrier free. Suitable for IHC-P, IP, WB and reacts with Human samples.
pH: 7.2 - 7.4
Constituents: PBS
IHC-P | IP | WB | ICC/IF | Flow Cyt (Intra) | |
---|---|---|---|---|---|
Human | Tested | Tested | Tested | Not recommended | Not recommended |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes For antigen retrieval: heat up to 98 degree C, below boiling, and then let cool for 10-20 min. Use of an HRP/AP polymerized secondary antibody is recommended. Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
C1s B chain is a serine protease that combines with C1q and C1r to form C1, the first component of the classical pathway of the complement system. C1r activates C1s so that it can, in turn, activate C2 and C4. Cleaves also IGFBP5 and thereby inhibits the trophic effects of IGF1.
Complement C1s subcomponent, C1 esterase, Complement component 1 subcomponent s, C1S
Rabbit Recombinant Monoclonal C1S antibody. Carrier free. Suitable for IHC-P, IP, WB and reacts with Human samples.
pH: 7.2 - 7.4
Constituents: PBS
ab248746 is the carrier-free version of Anti-C1s antibody [EPR9066(B)] ab134943.
Mouse, Rat: We have preliminary internal testing data to indicate this antibody may not react with these species. Please contact us for more information.
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
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.
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.
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.
This data was developed using Anti-C1s antibody [EPR9066(B)] ab134943, the same antibody clone in a different buffer formulation.Immunohistochemical analysis of paraffin-embedded, formalin-fixed Human liver tissue, labelling C1s using Anti-C1s antibody [EPR9066(B)] ab134943 at a 1/100 dilution. Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
This data was developed using Anti-C1s antibody [EPR9066(B)] ab134943, the same antibody clone in a different buffer formulation.Western blot analysis on Immunoprecipitation pellet from human plasma lysate using anti-C1s RabMAb (Anti-C1s antibody [EPR9066(B)] ab134943).
All lanes: Immunoprecipitation - Anti-C1s antibody [EPR9066(B)] (Anti-C1s antibody [EPR9066(B)] ab134943)
Predicted band size: 63 kDa, 77 kDa
Observed band size: 65 kDa
This data was developed using Anti-C1s antibody [EPR9066(B)] ab134943, the same antibody clone in a different buffer formulation.
All lanes: Western blot - Anti-C1s antibody [EPR9066(B)] (Anti-C1s antibody [EPR9066(B)] ab134943) at 1/1000 dilution
Lane 1: Human fetal kidney lysate at 10 µg
Lane 2: A431 cell lysate at 10 µg
Lane 3: Human platelet lysate at 10 µg
Lane 4: Human plasma lysate at 10 µg
Lane 5: Human serum lysate at 10 µg
All lanes: Standard HRP labelled goat anti-rabbit at 1/2000 dilution
Developed using the ECL technique.
Predicted band size: 77 kDa
C1s Western blot staining using rabbit Anti-C1s antibody
This data was developed using Anti-C1s antibody [EPR9066(B)] ab134943, the same antibody clone in a different buffer formulation.
Western blot: Rabbit Monoclonal[EPR9066(B)] to C1s Anti-C1s antibody [EPR9066(B)] ab134943 staining at 1/1000 dilution, shown in green; Mouse anti GAPDH (Anti-GAPDH antibody [6C5] - Loading Control ab8245) loading control staining at 1/20,000 dilution, shown in magenta. A band was observed at 77 kDa in Wild-type A549 cell lysates with no signal observed at this size in C1S knockout A549 cell line. To generate this image, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 3pc 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 800CW & Goat anti-Mouse 680RD at 1/20,000 dilution.
All lanes: Western blot - Anti-C1s antibody [EPR9066(B)] (Anti-C1s antibody [EPR9066(B)] ab134943) at 1/1000 dilution
Lane 1: Wild-type A549 at 20 µg
Lane 2: C1S knockout A549 at 20 µg
Lane 3: HEK-293 at 20 µg
Lane 4: Human Liver at 20 µg
All lanes: Goat anti-Rabbit 800CW & Goat anti-Mouse 680RD at 1/20000 dilution
Performed under reducing conditions.
Predicted band size: 77 kDa
Observed band size: 77 kDa
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