catalog number :
MBS8241844
products full name :
Anti-TUFM Antibody
products short name :
[TUFM]
products name syn :
[Elongation factor Tu, mitochondrial; EF-Tu; P43]
other names :
[Elongation factor Tu, mitochondrial; Elongation factor Tu, mitochondrial; elongation factor Tu, mitochondrial; Tu translation elongation factor, mitochondrial; P43]
products gene name :
[TUFM]
other gene names :
[TUFM; TUFM; P43; EFTU; COXPD4; EF-TuMT; EF-Tu]
uniprot entry name :
EFTU_HUMAN
reactivity :
Human, Mouse, Rat, Bovine, Dog, Monkey, Pig
specificity :
Recognizes endogenous levels of TUFM protein.
purity :
The antibody was purified by affinity chromatography.
form :
Liquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
storage stability :
Shipped at 4 degree C. Upon delivery aliquot and store at -20 degree C for one year. Avoid freeze/thaw cycles.
tested application :
Western Blot (WB), Immunohistochemistry (IHC)
app notes :
Western Blot: (1/500 - 1/1000); Immunohistochemistry: (1/100 - 1/200)
image1 heading :
Western Blot (WB)
image2 heading :
Immunohistochemistry (IHC)
other info1 :
Immunogen: KLH-conjugated synthetic peptide encompassing a sequence within the center region of human TUFM. The exact sequence is proprietary.
products description :
Rabbit polyclonal antibody to TUFM
ncbi pathways :
Mitochondrial Translation Pathway (1268842); Mitochondrial Translation Elongation Pathway (1268844); Organelle Biogenesis And Maintenance Pathway (1268838)
ncbi summary :
This gene encodes a protein which participates in protein translation in mitochondria. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency resulting in lactic acidosis and fatal encephalopathy. A pseudogene has been identified on chromosome 17. [provided by RefSeq, Jul 2008]
uniprot summary :
EFTU: This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis. Defects in TUFM are the cause of combined oxidative phosphorylation deficiency type 4 (COXPD4). COXPD4 is characterized by neonatal lactic acidosis, rapidly progressive encephalopathy, severely decreased mitochondrial protein synthesis, and combined deficiency of mtDNA-related mitochondrial respiratory chain complexes. Belongs to the GTP-binding elongation factor family. EF-Tu/EF-1A subfamily. Protein type: Translation elongation; RNA-binding; Translation; Mitochondrial. Chromosomal Location of Human Ortholog: 16p11.2. Cellular Component: membrane; mitochondrion. Molecular Function: GTP binding; GTPase activity; protein binding; translation elongation factor activity. Biological Process: mitochondrial translation; organelle organization and biogenesis; translational elongation. Disease: Combined Oxidative Phosphorylation Deficiency 4