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Products:Cell Biology >> Apoptosis >> Nucleus >> Other
MSCatalog No. MS103
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Read our guarantee »Anti-GRIM19 antibody
See all GRIM19 products (7) ...
Mouse monoclonal to GRIM19
WB, ICC/IF, ELISA, Flow Cytmore details
Reacts with
Mouse, Rat, Cow, Human
Recombinant full length protein Human GRIM19.
Human heart, Bovine heart, Rat heart, and Mouse heart isolated mitochondria, Human fibroblasts, HeLa cells
Liquid
Store at +4°C. Do not freeze.
Preservative: 0.02% Sodium azide
Constituent: HBS
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ab110240 was produced in vitro using hybridomas grown in serum-free medium, and then purified by biochemical fractionation.
Monoclonal
IgG2b
kappa
Metabolism >> Types of disease >> Cancer
Metabolism >> Pathways and Processes >> Metabolism processes >> Apoptosis
Metabolism >> Pathways and Processes >> Mitochondrial Metabolism >> Oxidative phosphorylation >> Complex I
Metabolism >> Pathways and Processes >> Metabolic signaling pathways >> Energy transfer pathways >> Integration of energy
Cancer >> Cancer Metabolism >> Metabolic signaling pathway >> Integration of energy metabolism
Epigenetics and Nuclear Signaling >> Cell cycle >> Apoptosis >> Nuclear
Cell Biology >> Apoptosis >> Nucleus >> Other
Our Abpromise guarantee covers the use of ab110240 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
WB: Use a concentration of 1 µg/ml. Predicted molecular weight: 17 kDa.
ICC/IF: Use a concentration of 1 µg/ml.
ELISA: Use a concentration of 8 µg/ml. In-Cell ELISA (0.8 µg/well)
Flow Cyt: Use a concentration of 1 µg/ml.
Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed not to be involved in catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. Involved in the interferon/all-trans-retinoic acid (IFN/RA) induced cell death. This apoptotic activity is inhibited by interaction with viral IRF1. Prevents the transactivation of STAT3 target genes. May play a role in CARD15-mediated innate mucosal responses and serve to regulate intestinal epithelial cell responses to microbes.
Widely expressed, with highest expression in heart, skeletal muscle, liver, kidney and placenta. In intestinal mucosa, down-regulated in areas involved in Crohn disease and ulcerative colitis.
Defects in NDUFA13 may be a cause of susceptibility to Hurthle cell thyroid carcinoma (HCTC) [MIM:607464]. Hurthle cell thyroid carcinoma accounts for approximately 3% of all thyroid cancers. Although they are classified as variants of follicular neoplasms, they are more often multifocal and somewhat more aggressive and are less likely to take up iodine than are other follicular neoplasms.
Belongs to the complex I NDUFA13 subunit family.
Expressed in numerous fetal tissues.
Mitochondrion inner membrane. Nucleus. May be translocated into the nucleus upon IFN/RA treatment.
Target information above from: UniProt accessionQ9P0J0
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - Anti-GRIM19 antibody (ab110240)

All lanes : Anti-GRIM19 antibody (ab110240) at 1 µg/ml
Lane 1 : Human heart mitochondria
Lane 2 : Bovine heart mitochondria
Lane 3 : Rat heart mitochondria
Lane 4 : Mouse heart mitochondria
Predicted band size : 17 kDa
Immunocytochemistry/ Immunofluorescence - Anti-GRIM19 antibody (ab110240)

Mitochondrial localization of GRIM19 visualized by immunocytochemistry using ab110240 at a concentration of 1 µg/mL. Cultured Human fibroblasts were fixed, permeabilized and then labeled with ab110240 followed by Alexa® 488 goat-anti-mouse IgG.
Flow Cytometry - Anti-GRIM19 antibody (ab110240)

HeLa cells were stained with 1 µg/mL ab110240 (blue) or an equal amount of an isotype control antibody (red) and analyzed by flow cytometry.
This product has been referenced in:
See all 12 publications for this product
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Mitochondrial localization of GRIM19 visualized by immunocytochemistry using ab110240 at a concentration of 1 µg/mL. Cultured Human fibroblasts were fixed, permeabilized and then labeled with ab110240 followed by Alexa® 488 goat-anti-mouse IgG.

HeLa cells were stained with 1 µg/mL ab110240 (blue) or an equal amount of an isotype control antibody (red) and analyzed by flow cytometry.
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