Anti-RIP antibody [EPR4689-100] - BSA and Azide free
- KO Validated
- RabMAb
- Recombinant
- What is this?
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(1 Publication)
Knockout Tested Rabbit Recombinant Monoclonal RIP antibody. Carrier free. Suitable for WB, Flow Cyt (Intra) and reacts with Human samples. Cited in 1 publication.
View Alternative Names
RIP, RIP1, RIPK1, Receptor-interacting serine/threonine-protein kinase 1, Cell death protein RIP, Receptor-interacting protein 1, RIP-1
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-RIP antibody [EPR4689-100] - BSA and Azide free (AB227843)
This Flow Cyt data was generated using the same anti-RIP antibody clone, EPR4689-100, in a different buffer formulation (cat
ab178420).
Intracellular flow cytometric analysis of permeabilized HeLa cells labeling RIP with ab178420 at 1/10 dilution (red) compared with a rabbit IgG negative control (green).
- WB
Unknown
Western blot - Anti-RIP antibody [EPR4689-100] - BSA and Azide free (AB227843)
This WB data was generated using the same anti-RIP antibody clone, EPR4689-100, in a different buffer formulation (cat# ab178420).
Lane 1 : Wild-type HAP1 cell lysate (20 μg)
Lane 2 : RIP knockout HAP1 cell lysate (20 μg)
Lane 3 : HeLa cell lysate (20 μg)
Lane 4 : Raji cell lysate (20 μg)
Lanes 1 to 4 : Merged signal (red and green). Green - ab178420 observed at 78 kDa. Red - loading control, ab8245, observed at 37 kDa.
ab178420 was shown to specifically react with RIP when RIP knockout samples were used. Wild-type and RIP knockout samples were subjected to SDS-PAGE. ab178420 and ab8245 (loading control to GAPDH) were both diluted 1/1000 and 1/10000 respectively and incubated overnight at 4°C. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) ab216773 and Goat anti-Mouse IgG H&L (IRDye® 680RD) ab216776 secondary antibodies at 1/10000 dilution for 1 h at room temperature before imaging.
All lanes:
Western blot - Anti-RIP antibody [EPR4689-100] (<a href='/en-us/products/primary-antibodies/rip-antibody-epr4689-100-ab178420'>ab178420</a>)
Predicted band size: 75 kDa
false
- WB
Lab
Western blot - Anti-RIP antibody [EPR4689-100] - BSA and Azide free (AB227843)
All lanes:
Western blot - Anti-RIP antibody [EPR4689-100] (<a href='/en-us/products/primary-antibodies/rip-antibody-epr4689-100-ab178420'>ab178420</a>) at 1/1000 dilution
Lanes 1 - 4:
Western blot - Human RIPK1 knockout THP-1 cell line (<a href='/en-us/products/cell-lines/human-ripk1-knockout-thp-1-cell-line-ab276121'>ab276121</a>)
Lane 1:
Wild-type THP-1 cell lysate at 20 µg
Lane 2:
RIPK1 knockout THP-1 cell lysate at 20 µg
Lane 3:
HeLa cell lysate at 20 µg
Lane 4:
Raji cell lysate at 20 µg
Predicted band size: 75 kDa
Observed band size: 76 kDa
true
- WB
Lab
Western blot - Anti-RIP antibody [EPR4689-100] - BSA and Azide free (AB227843)
This data was developed using the same antibody clone in a different buffer formulation (ab178420).
Western blot : Anti-RIPK1 antibody [EPR4689-100] (ab178420) staining at 1/1000 dilution, shown in green; Mouse anti-GAPDH antibody [6C5] (ab8245) loading control staining at 1/20000 dilution, shown in magenta. In Western blot, ab178420 was shown to bind specifically to RIPK1. A band was observed at 75 kDa in wild-type THP-1 cell lysates with no signal observed at this size in RIPK1 knockout cell line. To generate this image, wild-type and RIPK1 knockout THP-1 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-RIP antibody [EPR4689-100] (<a href='/en-us/products/primary-antibodies/rip-antibody-epr4689-100-ab178420'>ab178420</a>) at 1/1000 dilution
Lane 1:
Wild-type THP-1 cell lysate at 20 µg
Lane 2:
RIPK1 knockout THP-1 cell lysate at 20 µg
Lane 3:
Raji cell lysate at 20 µg
Lane 4:
HeLa cell lysate at 20 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: 75 kDa
Observed band size: 75 kDa
false
Related conjugates and formulations (1)
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Anti-RIP antibody [EPR4689-100]
Reactivity data
Product details
ab227843 is the carrier-free version of ab178420.
Species reactivity
Mouse, Rat: We have preliminary internal testing data to indicate this antibody may not react with these species.
Please contact us for more information.
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.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Receptor-Interacting Protein Kinase 1 (RIPK1) participates in regulating both necroptosis and apoptosis distinguishing itself as an important mediator in cell death mechanisms. As part of the necrosome complex which includes RIPK3 and MLKL RIPK1 functions in necroptosis—a programmed form of necrosis. This characteristic involvement shows its dual role in maintaining cell fate decisions making it an integral part of immune response and inflammation control.
Pathways
RIPK1 strongly associates with the TNF signaling pathway and NF-kB pathway. Its interaction with TNF receptor 1 (TNFR1) and consequent involvement with TRADD and TRAF2 mediates the signal transduction necessary for the activation of NF-kB leading to transcription of genes involved in survival and inflammation. This connection illustrates its capability to switch between promoting cell survival through NF-kB and facilitating cell death via necroptosis or apoptosis depending on cellular context and cues.
Product protocols
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Target data
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
International journal of nanomedicine 20:1083-1100 PubMed39895982
2025
Applications
Unspecified application
Species
Unspecified reactive species
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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