Recombinant Human TXNDC17/TRP14/TXNL5 Protein - PKSH031167 Size:100μg Mutations in this gene are

Mutations in this gene are associated with Leigh syndrome resulting from mitochondrial complex I deficiency

Mutations in this gene are a cause of autism spectrum disorder (ASD)

and mitochondrion

It is produced by monocytes

DF7176-200

Recombinant Human TXNDC17/TRP14/TXNL5 Protein - PKSH031167 Size:100μg Mutations in this gene areRecombinant Human TXNDC17 TRP14 TXNL5 Protein Size: 100g Catalogue Numbers: PKSH031167 100 Citations, Manuals and MSDS Available upon request. Abbreviation: TXNDC17; TRP14; TXNL5 Target Synonym: TRP14; TXNL5 UNIProt ID: Q9BRA2 Research Areas: Signal Transduction; Target Species: Human Expression Host: E. coli Fusion Tag: None Accession: Q9BRA2 Background: Cell surface A33 antigen, also known as glycoprotein A33, is a single pass type I membrane