Anti-MIF antibody [EPR12463]
- RabMAb
- Recombinant
- KO Validated
- What is this?
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(15 Publications)
Rabbit Recombinant Monoclonal MIF antibody. Suitable for IP, WB, Flow Cyt (Intra) and reacts with Human, Mouse, Rat samples. Cited in 15 publications.
View Alternative Names
GLIF, MMIF, MIF, Macrophage migration inhibitory factor, Glycosylation-inhibiting factor, L-dopachrome isomerase, L-dopachrome tautomerase, Phenylpyruvate tautomerase, GIF
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-MIF antibody [EPR12463] (AB175189)
Intracellular flow cytometric analysis of permeabilized Molt-4 cells using unpurified ab175189 at a 1/10 dilution (red) or a rabbit IgG (negative) (green).
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - Anti-MIF antibody [EPR12463] (AB175189)
Intracellular Flow Cytometry analysis of THP-1 cells labelling MIF with purified ab175189 at 1/140 (red). Cells were fixed with 2% paraformaldehyde. A FITC-conjugated goat anti-rabbit IgG (1/150) was used as the secondary anitbody. A rabbit monoclonal IgG was used as the isotype control (green).
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - Anti-MIF antibody [EPR12463] (AB175189)
Intracellular Flow Cytometry analysis of THP-1 cells labelling MIF with unpurified ab175189 at 1/50 (red). Cells were fixed with 2% paraformaldehyde. A FITC-conjugated goat anti-rabbit IgG (1/150) was used as the secondary anitbody. A rabbit monoclonal IgG was used as the isotype control (green).
- IP
Lab
Immunoprecipitation - Anti-MIF antibody [EPR12463] (AB175189)
ab175189 (unpurified) at 1/30 immunoprecipitating MIF in human fetal brain. For western blotting, a Peroxidase-conjugated goat anti-rabbit IgG (H+L) was used as the secondary antibody (1/1000).
Blocking buffer and concentration : 5% NFDM/TBST.
Diluting buffer and concentration : 5% NFDM /TBST.
All lanes:
Immunoprecipitation - Anti-MIF antibody [EPR12463] (ab175189)
Predicted band size: 12 kDa
Observed band size: 12 kDa
false
- IP
Lab
Immunoprecipitation - Anti-MIF antibody [EPR12463] (AB175189)
ab175189 (purified) at 1/50 immunoprecipitating MIF in human fetal brain. For western blotting, a Peroxidase-conjugated goat anti-rabbit IgG (H+L) was used as the secondary antibody (1/1000).
Blocking buffer and concentration : 5% NFDM/TBST.
Diluting buffer and concentration : 5% NFDM /TBST.
All lanes:
Immunoprecipitation - Anti-MIF antibody [EPR12463] (ab175189)
Predicted band size: 12 kDa
Observed band size: 12 kDa
false
- WB
Supplier Data
Western blot - Anti-MIF antibody [EPR12463] (AB175189)
All lanes:
Western blot - Anti-MIF antibody [EPR12463] (ab175189) at 1/1000 dilution
Lane 1:
Y79 lysates at 10 µg
Lane 2:
THP-1 lysates at 10 µg
Lane 3:
Molt-4 lysates at 10 µg
Lane 4:
Human fetal brain lysates at 10 µg
Predicted band size: 12 kDa
false
- WB
Unknown
Western blot - Anti-MIF antibody [EPR12463] (AB175189)
Blocking buffer and concentration : 5% NFDM/TBST.
Diluting buffer and concentration : 5% NFDM /TBST.
All lanes:
Western blot - Anti-MIF antibody [EPR12463] (ab175189) at 1/1000 dilution
Lane 1:
Y79 cell lysate at 20 µg/mL
Lane 2:
Mouse brain tissue lysate at 20 µg/mL
Lane 3:
Rat brain tissue lysate at 20 µg/mL
Secondary
All lanes:
Peroxidase-conjugated goat anti-rabbit IgG (H+L) at 1/1000 dilution
Predicted band size: 12 kDa
Observed band size: 12 kDa
false
- WB
Lab
Western blot - Anti-MIF antibody [EPR12463] (AB175189)
Lane 1 : Wild-type HAP1 whole cell lysate (20 μg)
Lane 2 : MIF knockout HAP1 whole cell lysate (20 μg)
Lane 3 : HeLa whole cell lysate (20 μg)
Lane 4 : HepG2 whole cell lysate (20 μg)
Lanes 1 - 4 : Merged signal (red and green). Green - ab175189 observed at 12 kDa. Red - loading control, ab9484, observed at 37 kDa.
ab175189 was shown to specifically react with MIF in wild-type HAP1 cells along with additional cross-reactive bands. No bands were observed when knockout cells were examined. Wild-type and MIF knockout samples were subjected to SDS-PAGE. ab175189 and ab9484 (Mouse anti GAPDH loading control) were incubated overnight at 4°C at 1/1000 dilution and 1/20,000 dilution respectively. Blots were developed 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 1/2,0000 dilution for 1 hour at room temperature before imaging.
All lanes:
Western blot - Anti-MIF antibody [EPR12463] (ab175189)
Predicted band size: 12 kDa
false
- WB
Lab
Western blot - Anti-MIF antibody [EPR12463] (AB175189)
Blocking buffer and concentration : 5% NFDM/TBST.
Diluting buffer and concentration : 5% NFDM /TBST.
All lanes:
Western blot - Anti-MIF antibody [EPR12463] (ab175189) at 1/2000 dilution
Lane 1:
Y79 cell lysate at 20 µg
Lane 2:
Mouse brain tissue lysate at 20 µg
Lane 3:
Rat brain tissue lysate at 20 µg
Secondary
All lanes:
Peroxidase-conjugated goat anti-rabbit IgG (H+L) at 1/1000 dilution
Predicted band size: 12 kDa
Observed band size: 12 kDa
false
Related conjugates and formulations (2)
-
HRP Anti-MIF antibody [EPR12463]
-
Anti-MIF antibody [EPR12463] - 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
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
MIF acts as an upstream regulator of innate immunity and exerts broad influence on cytokine release. MIF elevates pro-inflammatory cytokines like TNF-alpha and IL-1beta promoting an immune response. It does not typically form part of a complex but interacts with cell surface receptors like CD74 triggering intracellular signaling pathways. These interactions illustrate MIF as a regulator of immune cell recruitment and activation.
Pathways
MIF participates in the glucocorticoid receptor regulatory pathway and MAP kinase pathway. It shows interaction with JNK and ERK1/2 proteins which further map into important cellular reactions like stress response and cell proliferation. By integrating into these pathways MIF influences cell survival proliferation and inflammatory cascades emphasizing its role in immune regulation.
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
Target data
Publications (15)
Recent publications for all applications. Explore the full list and refine your search
Journal for immunotherapy of cancer 13: PubMed40846326
2025
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Molecular neurobiology 61:10481-10499 PubMed38743209
2024
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Molecular medicine reports 29: PubMed38639187
2024
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PLoS biology 19:e3001121 PubMed33661886
2021
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Advanced science (Weinheim, Baden-Wurttemberg, Germany) 8:2002874 PubMed33898171
2021
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Nature communications 10:903 PubMed30796225
2019
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The Journal of biological chemistry 293:19740-19760 PubMed30366984
2018
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European review for medical and pharmacological sciences 22:4908-4916 PubMed30070326
2018
Applications
WB
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International journal of molecular medicine 41:1062-1068 PubMed29207023
2017
Applications
WB
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Unspecified reactive species
Scientific reports 7:6361 PubMed28743960
2017
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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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