Anti-ING5 antibody [EPR23930-1] - BSA and Azide free
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal ING5 antibody. Carrier free. Suitable for ICC/IF, IP, WB, Flow Cyt (Intra) and reacts with Mouse, Human, Rat, Recombinant full length protein - Human samples.
View Alternative Names
Inhibitor of growth protein 5, p28ING5, ING5
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-ING5 antibody [EPR23930-1] - BSA and Azide free (AB277948)
This data was developed using ab259904, the same antibody clone in a different buffer formulation.
Intracellular flow cytometric analysis of 4% paraformaldehyde-fixed, 90% methanol-permeabilized HEK-293T (Human embryonic kidney epithelial cell) cells labelling ING5 with ab259904 at 1/500 dilution (0.1ug) (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue).
A Goat anti rabbit IgG (Alexa Fluor®488, ab150077) at 1/2000 dilution was used as the secondary antibody.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-ING5 antibody [EPR23930-1] - BSA and Azide free (AB277948)
This data was developed using ab259904, the same antibody clone in a different buffer formulation.
mmunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized HEK-293T cells labelling ING5 with ab259904 at 1/1000 (0.482 ug/ml) dilution, followed by ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) antibody at 1/1000 dilution (Green). Confocal image showing strong nuclear staining in HEK-293T cells. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 (Red). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution.
- IP
Supplier Data
Immunoprecipitation - Anti-ING5 antibody [EPR23930-1] - BSA and Azide free (AB277948)
This data was developed using ab259904, the same antibody clone in a different buffer formulation.
ING5 was immunoprecipitated from 0.35 mg MCF7 (human breast adenocarcinoma epithelial cell), whole cell lysate with ab259904 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab259904 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : MCF7 (human breast adenocarcinoma epithelial cell), whole cell lysate 10 ug
Lane 2 : ab259904 IP in MCF7 whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab259904 in MCF7 whole cell lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 10 seconds.
All lanes:
Immunoprecipitation - Anti-ING5 antibody [EPR23930-1] (<a href='/en-us/products/primary-antibodies/ing5-antibody-epr23930-1-ab259904'>ab259904</a>)
Predicted band size: 28 kDa
Observed band size: 32 kDa
false
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-ING5 antibody [EPR23930-1] - BSA and Azide free (AB277948)
This data was developed using ab259904, the same antibody clone in a different buffer formulation.
Intracellular flow cytometric analysis of 4% paraformaldehyde-fixed, 90% methanol-permeabilized NIH/3T3 (mouse embryonic fibroblast) cells labelling ING5 with ab259904 at 1/500 dilution (0.1ug) (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue).
A Goat anti rabbit IgG (Alexa Fluor®488, ab150077) at 1/2000 dilution was used as the secondary antibody.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-ING5 antibody [EPR23930-1] - BSA and Azide free (AB277948)
This data was developed using ab259904, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized NIH/3T3 cells labelling ING5 with ab259904 at 1/1000 (0.482 ug/ml) dilution, followed by ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) antibody at 1/1000 dilution (Green). Confocal image showing strong nuclear staining in NIH/3T3 cells. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 dilution (Red). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution.
- IP
Supplier Data
Immunoprecipitation - Anti-ING5 antibody [EPR23930-1] - BSA and Azide free (AB277948)
This data was developed using ab259904, the same antibody clone in a different buffer formulation.
ING5 was immunoprecipitated from 0.35 mg NIH/3T3 (mouse embryonic fibroblast), whole cell lysate with ab259904 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab259904 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : NIH/3T3 (mouse embryonic fibroblast), whole cell lysate 10 ug
Lane 2 : ab259904 IP in NIH/3T3 whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab259904 in NIH/3T3 whole cell lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 10 seconds.
All lanes:
Immunoprecipitation - Anti-ING5 antibody [EPR23930-1] (<a href='/en-us/products/primary-antibodies/ing5-antibody-epr23930-1-ab259904'>ab259904</a>)
Predicted band size: 28 kDa
Observed band size: 32 kDa
false
- WB
Lab
Western blot - Anti-ING5 antibody [EPR23930-1] - BSA and Azide free (AB277948)
This data was developed using ab259904, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Exposure times : Lane1-2 : 10 secondsLane3-4 : 15 seconds.
All lanes:
Western blot - Anti-ING5 antibody [EPR23930-1] (<a href='/en-us/products/primary-antibodies/ing5-antibody-epr23930-1-ab259904'>ab259904</a>) at 1/1000 dilution
Lane 1:
HEK-293T (human embryonic kidney epithelial cell), whole cell lysate at 20 µg
Lane 2:
HeLa (human cervix adenocarcinoma epithelial cell), whole cell lysate at 20 µg
Lane 3:
A549 (human lung carcinoma epithelial cell), whole cell lysate at 20 µg
Lane 4:
NIH/3T3 (mouse embryonic fibroblast), whole cell lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Predicted band size: 28 kDa
Observed band size: 32 kDa
false
- WB
Supplier Data
Western blot - Anti-ING5 antibody [EPR23930-1] - BSA and Azide free (AB277948)
This data was developed using ab259904, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST
Exposure time : Lane1-2 : 7.5 secondsLane3 : 70 seconds
All lanes:
Western blot - Anti-ING5 antibody [EPR23930-1] (<a href='/en-us/products/primary-antibodies/ing5-antibody-epr23930-1-ab259904'>ab259904</a>) at 1/1000 dilution
Lane 1:
MCF7 (human breast adenocarcinoma epithelial cell), whole cell lysate at 20 µg
Lane 2:
MDA-MB-231 (human breast adenocarcinoma epithelial cell), whole cell lysate at 20 µg
Lane 3:
C6 (rat glial tumor glial cell), whole cell lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Predicted band size: 28 kDa
Observed band size: 32 kDa
false
- WB
Lab
Western blot - Anti-ING5 antibody [EPR23930-1] - BSA and Azide free (AB277948)
This data was developed using ab259904, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Exposure times : Lane1 : 8 seconds; Lane2 : 3 minutes.
All lanes:
Western blot - Anti-ING5 antibody [EPR23930-1] (<a href='/en-us/products/primary-antibodies/ing5-antibody-epr23930-1-ab259904'>ab259904</a>) at 1/1000 dilution
Lane 1:
His-tagged human ING5 recombinant protein, 20 ng
Lane 2:
His-tagged human ING4 recombinant protein, 20 ng
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Predicted band size: 28 kDa
false
Reactivity data
Product details
ab277948 is the carrier-free version of ab259904.
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.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
ING5 plays a role in regulating cell cycle progression and maintaining genomic stability. It functions within the NuA4 histone acetyltransferase complex influencing chromatin remodeling and gene expression. ING5 interacts with several other proteins like p53 and p300/CBP contributing to its capability to suppress unwanted cellular proliferation. This makes it an important player in maintaining proper cell function and preventing malignant transformation.
Pathways
ING5 interacts with multiple proteins to contribute to the p53 signaling pathway and the DNA damage response pathway. It modulates p53-dependent transcriptional activity enhancing the cell's ability to respond to DNA damage. ING5’s role in these pathways links it to sister proteins in the ING family like ING1 and ING2 which also participate in p53-related responses and cell cycle control.
Product protocols
- Visit the General protocols
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Target data
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