catalog number :
MBS9212064
products full name :
ENOB Antibody (Center)
products short name :
[ENOB]
products name syn :
[Beta-enolase; 2-phospho-D-glycerate hydro-lyase; Enolase 3; Muscle-specific enolase; MSE; Skeletal muscle enolase; ENO3]
other names :
[beta-enolase isoform 2; Beta-enolase; beta-enolase; enolase 3 (beta, muscle); 2-phospho-D-glycerate hydro-lyase; Enolase 3; Muscle-specific enolase; MSE; Skeletal muscle enolase]
products gene name :
[ENO3]
other gene names :
[ENO3; ENO3; MSE; GSD13; MSE]
uniprot entry name :
ENOB_HUMAN
reactivity :
Human (Predicted Reactivity: Bovine, Mouse, Pig, Rat)
sequence positions :
[237-264]
specificity :
This ENOB antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 237-264 amino acids from the Central region of human ENOB.
purity :
Purified Rabbit Polyclonal Antibody (Pab)
form :
Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.
storage stability :
Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
tested application :
Western Blot (WB), Immunohistochemistry- Paraffin, Flow Cytometry (FC), ELISA (EIA)
app notes :
WB~~1:1000. IHC-P~~1:50~100. FC~~1:10~50
image1 heading :
Western Blot (WB)
image2 heading :
Immunohistochemistry (IHC)
image3 heading :
Flow Cytometry (FC/FACS)
other info1 :
Calculated MW: 46987
other info2 :
Function: Appears to have a function in striated muscle development and regeneration. Cellular Location: Cytoplasm. Note=Localized to the Z line. Some colocalization with CKM at M-band (By similarity. Tissue Location: The alpha/alpha homodimer is expressed in embryo and in most adult tissues. The alpha/beta heterodimer and the beta/beta homodimer are found in striated muscle, and the alpha/gamma heterodimer and the gamma/gamma homodimer in neurons.
products categories :
Crown Antibodies; Cancer; Metabolism; Signal Transduction
products description :
ENOB is one of the three enolase isoenzymes found in mammals. This isoenzyme, a homodimer, is found in skeletal muscle cells in the adult. A switch from alpha enolase to beta enolase occurs in muscle tissue during development in rodents. Mutations in its gene can be associated with metabolic myopathies that may result from decreased stability of the enzyme.
products references :
Aurino,S., Acta Myol 27, 90-97 (2008). Giallongo,A., Eur. J. Biochem. 214 (2), 367-374 (1993)
ncbi acc num :
NP_001180432.1
ncbi gb acc num :
NM_001193503.1
ncbi pathways :
Fatty Acid Biosynthesis Pathway (2027); Fatty Acid Biosynthesis Pathway (2027); Fatty Acid Biosynthesis Pathway (2027); Fatty Acid Biosynthesis Pathway (2027); Fatty Acid Biosynthesis Pathway (2027); Fatty Acid Biosynthesis Pathway (2027); Fatty Acid Biosynthesis Pathway (2027); Fatty Acid Biosynthesis Pathway (2027); Fatty Acid Biosynthesis Pathway (2027); Fatty Acid Biosynthesis Pathway (2027)
ncbi summary :
This gene encodes one of the three enolase isoenzymes found in mammals. This isoenzyme is found in skeletal muscle cells in the adult where it may play a role in muscle development and regeneration. A switch from alpha enolase to beta enolase occurs in muscle tissue during development in rodents. Mutations in this gene have be associated glycogen storage disease. Alternatively spliced transcript variants encoding different isoforms have been described.[provided by RefSeq, Jul 2010]
uniprot summary :
ENO3: Appears to have a function in striated muscle development and regeneration. Defects in ENO3 are the cause of glycogen storage disease type 13 (GSD13). A metabolic disorder that results in exercise-induced myalgias, generalized muscle weakness and fatigability. It is characterized by increased serum creatine kinase and decreased enolase 3 activity. Dramatically reduced protein levels with focal sarcoplasmic accumulation of glycogen- beta particles are detected on ultrastructural analysis. Belongs to the enolase family. 3 isoforms of the human protein are produced by alternative splicing. Protein type: EC 4.2.1.11; Carbohydrate Metabolism - glycolysis and gluconeogenesis; Lyase. Chromosomal Location of Human Ortholog: 17p13.2. Cellular Component: extracellular space; phosphopyruvate hydratase complex; cytoplasm; plasma membrane; cytosol. Molecular Function: protein homodimerization activity; protein heterodimerization activity; magnesium ion binding; phosphopyruvate hydratase activity. Biological Process: response to drug; glycolysis; carbohydrate metabolic process; skeletal muscle regeneration; glucose metabolic process; pathogenesis; aging; gluconeogenesis. Disease: Glycogen Storage Disease Xiii