Anti-SET/TAF-I antibody [EPR12972(B)]
- RabMAb
- Recombinant
- What is this?
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(2 Publications)
Rabbit Recombinant Monoclonal SET/TAF-I antibody. Suitable for IP, WB, Flow Cyt (Intra) and reacts with Human samples. Cited in 2 publications.
View Alternative Names
Protein SET, HLA-DR-associated protein II, Inhibitor of granzyme A-activated DNase, PHAPII, Phosphatase 2A inhibitor I2PP2A, Template-activating factor I, IGAAD, I-2PP2A, TAF-I, SET
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-SET/TAF-I antibody [EPR12972(B)] (AB176567)
Intracellular Flow Cytometry analysis of permeabilized Jurkat cells labeling SET/TAF-I (red) with ab176567 at a 1/10 dilution, or negative control rabbit IgG (green)
- IP
Supplier Data
Immunoprecipitation - Anti-SET/TAF-I antibody [EPR12972(B)] (AB176567)
Western blot analysis on immunoprecipitation pellet from HeLa cell lysate labeling SET/TAF-I with ab176567 at 1/10 dilution.
All lanes:
Immunoprecipitation - Anti-SET/TAF-I antibody [EPR12972(B)] (ab176567)
Predicted band size: 33 kDa
true
- WB
Supplier Data
Western blot - Anti-SET/TAF-I antibody [EPR12972(B)] (AB176567)
All lanes:
Western blot - Anti-SET/TAF-I antibody [EPR12972(B)] (ab176567) at 1/10000 dilution
Lane 1:
Jurkat cell lysate at 10 µg
Lane 2:
293T (Human embryonic kidney epithelial cell) cell lysate at 10 µg
Lane 3:
HepG2 cell lysate at 10 µg
Lane 4:
HeLa cell lysate at 10 µg
Secondary
All lanes:
Goat anti-rabbit HRP at 1/2000 dilution
Predicted band size: 33 kDa
true
Related conjugates and formulations (1)
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Anti-SET/TAF-I antibody [EPR12972(B)] - BSA and Azide free
Reactivity data
Product details
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.
Properties and storage information
Form
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
In the context of cellular processes SET/TAF-I functions as a histone chaperone and is a part of the nucleosome assembly complex. This protein is involved in nucleosome disassembly and assembly during DNA replication and repair and it modulates transcriptional access for various transcription factors. It regulates the acetylation of histones influencing gene expression levels. The SET/TAF-I also participates in apoptosis and autophagy demonstrating its versatility in cellular control mechanisms.
Pathways
Studies show that SET/TAF-I engages in the MAPK/ERK signaling pathway which is critical for cell cycle progression and proliferation. It is linked with other proteins such as HMGN proteins and histone deacetylases playing a substantial role in chromatin dynamics and genomic stability. Furthermore SET/TAF-I is central to the signaling pathway that maintains normal cellular functions and responds to stress signals like oxidative stress demonstrating its importance in normal cell regulation.
Product protocols
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Target data
Publications (2)
Recent publications for all applications. Explore the full list and refine your search
Cell reports 30:3171-3182.e6 PubMed32130916
2020
Applications
Unspecified application
Species
Unspecified reactive species
Nature immunology 17:556-64 PubMed26974206
2016
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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