recommended for detection of TFB1M of human origin by WB, IP and ELISA
Modification Notes
TFB1M (transcription factor B1, mitochondrial), also known as CGI75, mtTFB or CGI-75, is a 346 amino acid mitochondrial protein that, along with mtTFA and MtRPOL, is required for the transcription of genes from mitochondrial DNA. Expressed ubiquitously, TFB1M functions as an S-adenosyl-L-methionine-dependent methyltransferase that specifically dimethylates mitochondrial 12S rRNA at the conserved stem loop and is required for mitochondrial DNA transcription. Variations in the gene encoding TFB1M are thought to influence the pathogenesis of aminoglycoside-induced deafness (AID), a disorder that is characterized by hearing loss and is caused by irregular methylation of 12S rRNA. The gene encoding TFB1M maps to human chromosome 6, which contains 170 million base pairs and comprises nearly 6% of the human genome.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPELISA
WB:1:500~1:2000 IP:1:100~1:500 Notes:Optimal dilutions/concentrations should be determined by the researcher.
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
recommended for detection of TFB1M of human origin by WB IP and ELISA
Tissue Specificity
recommended for detection of TFB1M of human origin by WB, IP and ELISA