SYFM Rabbit Polyclonal Antibody

Ab type

Primary antibody

Background

This gene encodes a protein that transfers phenylalanine to its cognate tRNA. This protein localizes to the mitochondrion and plays a role in mitochondrial protein translation. Mutations in this gene can cause combined oxidative phosphorylation deficiency 14 (Alpers encephalopathy). Alternative splicing results in multiple transcript variants.

Reactivity

Human, Mouse, Rat

Clonality

Polyclonal

Host

Rabbit

Isotype

IgG

Immunogen

Synthesized peptide derived from human SYFM

Storage Stability

-20°C for 1 year

Concentration

1 mg/ml

MolecularWeight_Da

49610

synonyms

SYFM