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Rabbit Anti-UQCC2 Antibody (CSB-PA866268ESR2HU)
Supplier: CUSABIO BIOTECH CO.
Ubiquinol-cytochrome-c reductase complex assembly factor 2 Antibody,Breast cancer-associated protein SGA-81M Antibody,Mitochondrial nucleoid factor 1 Antibody,Mitochondrial protein M19 Antibody,UQCC2 Antibody,C6orf125 Antibody,MNF1 AntibodyMore alternative names for the antibody
bA6B20.2 antibody|Breast cancer-associated protein SGA-81M antibody|C6orf125 antibody|Cbp6 antibody|M19 antibody|Mitochondrial nucleoid factor 1 antibody|Mitochondrial protein M19 antibody|MNF1 antibody|RP11-6B20.2 antibody
Anti-MNF1 antibody (ab150849)
Anti-MNF1 antibody (ab150849)
Recommended applications: ELISA, WB, IHC
Recommended dilution: User optimized
Recommended protocols: check protocols
|Catalogue No.|| |
Recombinant human Ubiquinol-cytochrome-c reductase complex assembly factor 2 protein (14-126AA)
ELISA, WB, IHC
|Recommended dilution|| |
|Molecular weight|| |
Antigen Affinity Purified
Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.
|Protein function|| |
Required for the assembly of the ubiquinol-cytochrome c reductase complex (mitochondrial respiratory chain complex III or cytochrome b-c1 complex). Plays a role in the modulation of respiratory chain activities such as oxygen consumption and ATP production and via its modulation of the respiratory chain activity can regulate skeletal muscle differentiation and insulin secretion by pancreatic beta-cells. Involved in cytochrome b translation and/or stability. .
|Protein tissue specificity|| |
Pancreas, skeletal muscle, kidney, liver and heart. .
|Involvement in disease|| |
Mitochondrial complex III deficiency, nuclear 7 (MC3DN7) [MIM:615824]: A form of mitochondrial complex III deficiency, a disorder of the mitochondrial respiratory chain resulting in a highly variable phenotype depending on which tissues are affected. MC3DN7 is characterized by severe intrauterine growth retardation, neonatal lactic acidosis and renal tubular dysfunction. Additional clinical features include a dysmorphic facial appearance, delayed psychomotor development, autistic features, aggressive behavior, and mild sensorineural hearing loss. . Note=The disease is caused by mutations affecting the gene represented in this entry.
|Protein cellular localization|| |
Mitochondrion matrix, mitochondrion nucleoid. Mitochondrion. Mitochondrion intermembrane space . Mitochondrion matrix . Mitochondrion inner membrane . Note=Predominantly expressed in the mitochondrial inner membrane. .
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CUSABIO BIOTECH CO.
|Product type|| |
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