CCDC44 MaxPab mouse polyclonal antibody (B01)
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More Files
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Specification
Product Description
Mouse polyclonal antibody raised against a full-length human CCDC44 protein.
Immunogen
CCDC44 (NP_057444.2, 1 a.a. ~ 297 a.a) full-length human protein.
Sequence
MSAWAAASLSRAAARCLLARGPGVRAAPPRDPRPSHPEPRGCGAAPGRTLHFTAAVPAGHNKWSKVRHIKGPKDVERSRIFSKLCLNIRLAVKEGGPNPEHNSNLANILEVCRSKHMPKSTIETALKMEKSKDTYLLYEGRGPGGSSLLIEALSNSSHKCQADIRHILNKNGGVMAVGARHSFDKKGVIVVEVEDREKKAVNLERALEMAIEAGAEDVKETEDEEERNVFKFICDASSLHQVRKKLDSLGLCSVSCALEFIPNSKVQLAEPDLEQAAHLIQALSNHEDVIHVYDNIE
Host
Mouse
Reactivity
Human
Interspecies Antigen Sequence
Rat (77)
Quality Control Testing
Antibody reactive against mammalian transfected lysate.
Storage Buffer
No additive
Storage Instruction
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
Note
For IHC and IF applications, antibody purification with Protein A will be needed prior to use.
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Applications
Western Blot (Transfected lysate)
Western Blot analysis of CCDC44 expression in transfected 293T cell line (H00051204-T01) by CCDC44 MaxPab polyclonal antibody.
Lane 1: CCDC44 transfected lysate(32.67 KDa).
Lane 2: Non-transfected lysate.
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Gene Info — CCDC44
Entrez GeneID
51204GeneBank Accession#
NM_016360.2Protein Accession#
NP_057444.2Gene Name
CCDC44
Gene Alias
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Gene Description
coiled-coil domain containing 44
Gene Ontology
HyperlinkGene Summary
TACO1 is a mitochondrial translational activator required for efficient translation of cytochrome c oxidase (COX) subunit I (MTCO1; MIM 516030) (Weraarpachai et al., 2009), a component of complex IV of the mitochondrial respiratory complex.[supplied by OMIM
Other Designations
clone HQ0477 PRO0477p
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Interactome
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Publication Reference
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A mutation in the FAM36A gene, the human ortholog of COX20, impairs cytochrome c oxidase assembly and is associated with ataxia and muscle hypotonia.
Szklarczyk R, Wanschers BF, Nijtmans LG, Rodenburg RJ, Zschocke J, Dikow N, van den Brand MA, Hendriks-Franssen MG, Gilissen C, Veltman JA, Nooteboom M, Koopman WJ, Willems PH, Smeitink JA, Huynen MA, van den Heuvel LP.
Human Molecular Genetics 2013 Feb; 22(4):656.
Application:WB-Ce, Human, Fibroblasts.
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A mutation in the FAM36A gene, the human ortholog of COX20, impairs cytochrome c oxidase assembly and is associated with ataxia and muscle hypotonia.
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