Anti-UFC1 antibody [EPR15014]
- RabMAb
- Recombinant
- KO Validated
- What is this?
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(8 Publications)
Rabbit Recombinant Monoclonal UFC1 antibody. Suitable for WB, IHC-P and reacts with Rat, Human, Mouse samples. Cited in 8 publications.
View Alternative Names
CGI-126, HSPC155, UFC1, Ubiquitin-fold modifier-conjugating enzyme 1, Ufm1-conjugating enzyme 1
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-UFC1 antibody [EPR15014] (AB189251)
Immunohistochemical analysis of paraffin-embedded Human colon tissue labeling UFC1 with ab189251 at 1/100 dilution, followed by prediluted HRP Polymer for Rabbit IgG. Counter stained with hematoxylin.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-UFC1 antibody [EPR15014] (AB189251)
Immunohistochemical analysis of paraffin-embedded Human hepatocellular carcinoma tissue labeling UFC1 with ab189251 at 1/100 dilution, followed by prediluted HRP Polymer for Rabbit IgG. Counter stained with hematoxylin.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- WB
Lab
Western blot - Anti-UFC1 antibody [EPR15014] (AB189251)
Lanes 1 - 4 : Merged signal (red and green). Green - ab189251 observed at 20 kDa. Red - loading control, ab8245 (Mouse anti-GAPDH antibody [6C5]) observed at 37kDa.
ab189251 was shown to react with UFC1 in wild-type HAP1 cells in Western blot. Loss of signal was observed when UFC1 knockout sample was used. Wild-type HAP1 and UFC1 knockout cell lysates were subjected to SDS-PAGE. Membranes were blocked in 3% milk in TBS-T (0.1% Tween®) before incubation with ab189251 and ab8245 (Mouse anti-GAPDH antibody [6C5]) overnight at 4°C at a 1 in 10000 dilution and a 1 in 20000 dilution respectively. Blots were incubated with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed (ab216776) secondary antibodies at 1 in 20000 dilution for 1 hour at room temperature before imaging.
All lanes:
Western blot - Anti-UFC1 antibody [EPR15014] (ab189251) at 1/10000 dilution
Lane 1:
Wild-type HAP1 cell lysate at 20 µg
Lane 2:
UFC1 knockout HAP1 cell lysate at 20 µg
Lane 3:
MCF7 cell lysate at 20 µg
Lane 4:
A549 cell lysate at 20 µg
Predicted band size: 19 kDa
Observed band size: 20 kDa
false
- WB
Lab
Western blot - Anti-UFC1 antibody [EPR15014] (AB189251)
Lanes 1- 2 : Merged signal (red and green). Green - ab189251 observed at 20 kDa. Red - Anti-GAPDH antibody [6C5] - Loading Control (ab8245) observed at 37 kDa.
ab189251 was shown to react with UFC1 in wild-type HEK-293T cells in western blot. Loss of signal was observed when knockout cell line ab266814 (knockout cell lysate ab257781) was used. Wild-type HEK-293T and UFC1 HEK-293T KO cell lysates were subjected to SDS-PAGE. Membrane was blocked for 1 hour at room temperature in 0.1% TBST with 3% non-fat dried milk. ab189251 and Anti-GAPDH antibody [6C5] - Loading Control (ab8245) overnight at 4°C at a 1 in 10000 dilution and a 1 in 20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye®800CW) preadsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye®680RD) preadsorbed (ab216776) secondary antibodies at 1 in 20000 dilution for 1 hour at room temperature before imaging.
All lanes:
Western blot - Anti-UFC1 antibody [EPR15014] (ab189251) at 1/10000 dilution
Lane 1:
Wild-type HEK-293T cell lysate at 20 µg
Lane 2:
UFC1 knockout HEK-293T cell lysate at 20 µg
Lane 2:
Western blot - Human UFC1 knockout HEK-293T cell line (<a href='/en-us/products/cell-lines/human-ufc1-knockout-hek-293t-cell-line-ab266814'>ab266814</a>)
Predicted band size: 19 kDa
Observed band size: 20 kDa
false
- WB
Supplier Data
Western blot - Anti-UFC1 antibody [EPR15014] (AB189251)
All lanes:
Western blot - Anti-UFC1 antibody [EPR15014] (ab189251) at 1/20000 dilution
Lane 1:
Human fetal liver lysate at 20 µg
Lane 2:
A549 cell lysate at 20 µg
Lane 3:
U-87 MG cell lysate at 20 µg
Lane 4:
MCF7 cell lysate at 20 µg
Secondary
All lanes:
Goat anti-rabbit IgG, (H+L), peroxidase conjugate at 1000 µg
Predicted band size: 19 kDa
Observed band size: 19 kDa
false
- WB
Supplier Data
Western blot - Anti-UFC1 antibody [EPR15014] (AB189251)
All lanes:
Western blot - Anti-UFC1 antibody [EPR15014] (ab189251) at 1/5000 dilution
Lane 1:
C6 cell lysate at 10 µg
Lane 2:
Raw 264.7 cell lysate at 10 µg
Lane 3:
PC12 cell lysate at 10 µg
Lane 4:
NIH 3T3 cell lysate at 10 µg
Secondary
All lanes:
Goat anti-rabbit IgG, (H+L), peroxidase conjugate at 1/1000 dilution
Predicted band size: 19 kDa
Observed band size: 19 kDa
false
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
Purification technique
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
UFC1 is involved in the process of UFMylation which modifies proteins through the attachment of UFM1 much like ubiquitination influences protein degradation and signaling. UFC1 forms part of a complex that also includes UBA5 and UFL1 the E1 activating enzyme and E3 ligase respectively. This UFMylation system is necessary for endoplasmic reticulum-associated degradation (ERAD) contributing to the maintenance of protein homeostasis within cells. The disruption of this modification process can impact cellular stress response and protein quality control mechanisms.
Pathways
UFC1 plays a critical role in the ER stress response and protein quality control pathways. Within these pathways UFC1 interacts with proteins such as UFM1 and UFL1 to mediate the UFMylation of target proteins during cellular stress. Additionally UFC1 has been linked to pathways regulating autophagy where it indirectly influences the degradation of defective proteins. This interaction ultimately affects the cellular response to misfolded proteins and is pivotal for maintaining cellular equilibrium.
Product protocols
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Target data
Publications (8)
Recent publications for all applications. Explore the full list and refine your search
Cell reports methods 5:101048 PubMed40347946
2025
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Autophagy 21:996-1018 PubMed39842454
2025
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Cell death & disease 15:544 PubMed39085203
2024
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Nature 627:445-452 PubMed38383785
2024
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Cell reports 40:111168 PubMed35926457
2022
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International journal of molecular sciences 22: PubMed34299007
2021
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Brain : a journal of neurology 141:1934-1945 PubMed29868776
2018
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American journal of human genetics 99:695-703 PubMed27545681
2016
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Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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