Description
Antibody Name: | COQ4 Antibody (PACO42726) |
Antibody SKU: | PACO42726 |
Size: | 50ug |
Host Species: | Rabbit |
Tested Applications: | ELISA, IHC |
Recommended Dilutions: | ELISA:1:2000-1:10000, IHC:1:20-1:200 |
Species Reactivity: | Human |
Immunogen: | Recombinant Human Ubiquinone biosynthesis protein COQ4 homolog, mitochondrial protein (31-265AA) |
Form: | Liquid |
Storage Buffer: | Preservative: 0.03% Proclin 300 Constituents: 50% Glycerol, 0.01M PBS, PH 7.4 |
Purification Method: | >95%, Protein G purified |
Clonality: | Polyclonal |
Isotype: | IgG |
Conjugate: | Non-conjugated |
Immunohistochemistry of paraffin-embedded human liver tissue using PACO42726 at dilution of 1:100. | |
Immunohistochemistry of paraffin-embedded human spleen tissue using PACO42726 at dilution of 1:100. |
Background: | Component of the coenzyme Q biosynthetic pathway. May play a role in organizing a multi-subunit COQ enzyme complex required for coenzyme Q biosynthesis. Required for steady-state levels of other COQ polypeptides. |
Synonyms: | Ubiquinone biosynthesis protein COQ4 homolog, mitochondrial (Coenzyme Q biosynthesis protein 4 homolog), COQ4 |
UniProt Protein Function: | COQ4: Component of the coenzyme Q biosynthetic pathway. May play a role in organizing a multi-subunit COQ enzyme complex required for coenzyme Q biosynthesis. Required for steady-state levels of other COQ polypeptides. Belongs to the COQ4 family. 2 isoforms of the human protein are produced by alternative splicing.Protein type: MitochondrialChromosomal Location of Human Ortholog: 9q34.11Cellular Component: mitochondrionBiological Process: ubiquinone biosynthetic processDisease: Coenzyme Q10 Deficiency, Primary, 7 |
UniProt Protein Details: | |
NCBI Summary: | This gene encodes a component of the coenzyme Q biosynthesis pathway. Coenzyme Q, an essential component of the electron transport chain, shuttles electrons between complexes I or II to complex III of the mitochondrial transport chain. This protein appears to play a structural role in stabilizing a complex that contains most of the coenzyme Q biosynthesis enzymes. Mutations in this gene are associated with mitochondrial disorders linked to coenzyme Q deficiency. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015] |
UniProt Code: | Q9Y3A0 |
NCBI GenInfo Identifier: | 40225458 |
NCBI Gene ID: | 51117 |
NCBI Accession: | BC011895 |
UniProt Secondary Accession: | Q9Y3A0,Q5T4B8, Q96EW4, A8WBK8, B2R958 |
UniProt Related Accession: | Q9Y3A0 |
Molecular Weight: | 27,043 Da |
NCBI Full Name: | Homo sapiens coenzyme Q4 homolog (S. cerevisiae), mRNA |
NCBI Synonym Full Names: | coenzyme Q4 |
NCBI Official Symbol: | COQ4 |
NCBI Official Synonym Symbols: | CGI-92; COQ10D7 |
NCBI Protein Information: | ubiquinone biosynthesis protein COQ4 homolog, mitochondrial |
UniProt Protein Name: | Ubiquinone biosynthesis protein COQ4 homolog, mitochondrial |
UniProt Synonym Protein Names: | Coenzyme Q biosynthesis protein 4 homolog |
Protein Family: | Ubiquinone biosynthesis protein |
UniProt Gene Name: | COQ4 |
UniProt Entry Name: | COQ4_HUMAN |