SYFM rabbit pAb
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. [provided by RefSeq, Jan 2016],
Product Specifications
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. [provided by RefSeq, Jan 2016]
UniProt
O95363
Swiss Prot
O95363
Reactivity
Human; Mouse; Rat
Immunogen
Synthesized peptide derived from human SYFM AA range: 294-344
Target
SYFM
Clonality
Polyclonal
Source
Rabbit
Applications
WB; ELISA; IHC
Concentration
1 mg/ml
Dilution
WB 1:500-2000; IHC-p 1:50-300; ELISA 2000-20000
Buffer
-20°C/1 year
Storage Conditions
-20°C/1 year
Fragment
IgG
Subcellular Location
Mitochondrion matrix . Mitochondrion .
Gene ID (Human)
10667
Available Sizes
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