Description
Product Name: | Human TACO1 Recombinant Protein |
Product Code: | RPPB4896 |
Size: | 20µg |
Species: | Human |
Target: | TACO1 |
Synonyms: | Translational Activator Of Mitochondrially Encoded Cytochrome C Oxidase, CCDC44, Coiled-Coil Domain-Containing Protein 44, Coiled-Coil Domain Containing 44, Clone HQ0477 PRO0477p, Translational Activator Of Cytochrome C Oxidase 1, Translational Activator Of Mitochondrially-Encoded Cytochrome C Oxidase I. |
Source: | Escherichia Coli |
Physical Appearance: | Sterile Filtered clear solution. |
Formulation: | TACO1 protein solution (0.5mg/ml) containing 20mMTris-HCl buffer (pH 8.0), 0.15M NaCl, 10% glycerol and 1mM DTT. |
Stability: | Store at 4°C if entire vial will be used within 2-4 weeks. Store, frozen at -20°C for longer periods of time.For long term storage it is recommended to add a carrier protein (0.1% HSA or BSA).Please avoid freeze thaw cycles. |
Purity: | Greater than 95% as determined by SDS-PAGE. |
Amino Acid Sequence: | MGSSHHHHHH SSGLVPRGSH MGSNKWSKVR HIKGPKDVER SRIFSKLCLN IRLAVKEGGP NPEHNSNLAN ILEVCRSKHM PKSTIETALK MEKSKDTYLL YEGRGPGGSS LLIEALSNSS HKCQADIRHI LNKNGGVMAV GARHSFDKKG VIVVEVEDRE KKAVNLERAL EMAIEAGAEDVKETEDEEER NVFKFICDAS SLHQVRKKLD SLGLCSVSCA LEFIPNSKVQ LAEPDLEQAA HLIQALSNHE DVIHVYDNIE |
Translationalactivator of mitochondrially encoded cytochrome c oxidase I (TACO1) belongs tothe TACO1 family. TACO1 is a mitochondrial protein which functions as atranslational activator of mitochondrially-encoded cytochrome c oxidase 1. Mutationsin this gene are associated with Leigh syndrome.
TACO1 Human Recombinant produced in E.Coli is a single, non-glycosylated polypeptide chain containing 260 amino acids (61-297 a.a) and having a molecular mass of 28.8kDa.TACO1 is fused to a 23 amino acid His-tag at N-terminus & purified by proprietary chromatographic techniques.
UniProt Protein Function: | CCDC44: Acts as a translational activator of mitochondrially- encoded cytochrome c oxidase 1. Defects in TACO1 are a cause of Leigh syndrome (LS). LS is a severe neurological disorder characterized by bilaterally symmetrical necrotic lesions in subcortical brain regions that is commonly associated with systemic cytochrome c oxidase (COX) deficiency. Belongs to the TACO1 family. |
UniProt Protein Details: | Chromosomal Location of Human Ortholog: 17q23.3 Cellular Component: mitochondrion; nucleus Disease: Mitochondrial Complex Iv Deficiency |
NCBI Summary: | This gene encodes a mitochondrial protein that function as a translational activator of mitochondrially-encoded cytochrome c oxidase 1. Mutations in this gene are associated with Leigh syndrome.[provided by RefSeq, Mar 2010] |
UniProt Code: | Q9BSH4 |
NCBI GenInfo Identifier: | 33516968 |
NCBI Gene ID: | 51204 |
NCBI Accession: | Q9BSH4.1 |
UniProt Secondary Accession: | Q9BSH4,Q8N3N6, Q9UI60, B2RD21, |
UniProt Related Accession: | Q9BSH4 |
Molecular Weight: | 32,477 Da |
NCBI Full Name: | Translational activator of cytochrome c oxidase 1 |
NCBI Synonym Full Names: | translational activator of cytochrome c oxidase I |
NCBI Official Symbol: | TACO1�� |
NCBI Official Synonym Symbols: | CCDC44�� |
NCBI Protein Information: | translational activator of cytochrome c oxidase 1 |
UniProt Protein Name: | Translational activator of cytochrome c oxidase 1 |
UniProt Synonym Protein Names: | Coiled-coil domain-containing protein 44; Translational activator of mitochondrially-encoded cytochrome c oxidase I |
Protein Family: | Translational activator of cytochrome c oxidase |
UniProt Gene Name: | TACO1�� |
UniProt Entry Name: | TACO1_HUMAN |