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Rabbit Anti-RSFA/FITC Conjugated antibody
background:
C18orf22, also known as HsT169, is a 343 amino acid protein that localizes to the mitochondrion and is expressed as two alternatively spliced isoforms that are encoded by a gene which maps to human chromosome 18. Chromosome 18 houses over 300 protein-coding genes and contains nearly 76 million nucleotide bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.
Subcellular Location:
Mitochondrion.
Similarity:
Belongs to the RbfA family.
Database links:
Entrez Gene: 79863 Human
SwissProt: Q8N0V3 Human
Unigene: 593610 Human
Unigene: 728931 Human
Unigene: 729952 Human
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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