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Anti-Non Neuronal Enolase antibody
See all Non Neuronal Enolase products (8) ...
Rabbit polyclonal to Non Neuronal Enolase
This antibody is specific for Non Neuronal Enolase.
IHC-P, WB, IHC-Fr, ICC/IFmore details
Reacts with
Mouse, Human
Predicted to work with
Rat, Pig, Zebrafish
A synthetic peptide corresponding to a region of Human Non Neuronal Enolase, derived from within the following sequence (aa 246-295): VAASEFFRSG KYDLDFKSPD DPSRYISPDQ LADLYKSFIK DYPVVSIEDP.
Fetal Intestine lysate and human kidney tissue
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
Preservative: None
Constituents: 2% Sucrose, PBS
Concentration information loading...
Immunogen affinity purified
Polyclonal
IgG
Cancer >> Cancer Metabolism >> Response to hypoxia
Cancer >> Cancer Metabolism >> Metabolic signaling pathway >> Metabolism of carbohydrates
Cancer >> Oncoproteins/suppressors >> Tumor suppressors >> Other
Epigenetics and Nuclear Signaling >> Transcription >> Co-factors
Epigenetics and Nuclear Signaling >> Transcription >> Transcription Factors
Epigenetics and Nuclear Signaling >> Transcription >> Other factors
Epigenetics and Nuclear Signaling >> Transcription >> Cancer susceptibility >> Tumor Suppressors
Signal Transduction >> Metabolism >> Energy Metabolism
Our Abpromise guarantee covers the use of ab49343 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
IHC-P: Use a concentration of 4 - 8 µg/ml.
WB: Use a concentration of 0.03 µg/mlDetects a band of approximately 47 kDa (predicted molecular weight: 47 kDa).
IHC-Fr: 1/250
ICC/IF: Use a concentration of 1 µg/ml
Multifunctional enzyme that, as well as its role in glycolysis, plays a part in various processes such as growth control, hypoxia tolerance and allergic responses. May also function in the intravascular and pericellular fibrinolytic system due to its ability to serve as a receptor and activator of plasminogen on the cell surface of several cell-types such as leukocytes and neurons. Stimulates immunoglobulin production.
MBP1 binds to the myc promoter and acts as a transcriptional repressor. May be a tumor suppressor.
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.
Carbohydrate degradation; glycolysis; pyruvate from D-glyceraldehyde 3-phosphate: step 4/5.
Belongs to the enolase family.
During ontogenesis, there is a transition from the alpha/alpha homodimer to the alpha/beta heterodimer in striated muscle cells, and to the alpha/gamma heterodimer in nerve cells.
ISGylated.
Nucleus and Cytoplasm. Cell membrane. Cytoplasm > myofibril > sarcomere > M line. Can translocate to the plasma membrane in either the homodimeric (alpha/alpha) or heterodimeric (alpha/gamma) form. ENO1 is localized to the M line.
Target information above from: UniProt accessionP06733
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - Non Neuronal Enolase antibody (ab49343)

Anti-Non Neuronal Enolase antibody (ab49343) at 0.03 µg/ml + Fetal intestine lysate 10µg
Secondary
HRP conjugated anti-Rabbit IgG at 1/50000 dilution
Predicted band size : 47 kDa
Observed band size : 47 kDa
Immunohistochemistry (Paraffin-embedded sections) - Non Neuronal Enolase antibody (ab49343)

ab49343 at 4µg/ml staining Non Neuronal Enolase in epithelial cells of collecting tubules (arrows) of human kidney tissue.
Immunohistochemistry (Frozen sections) - Non Neuronal Enolase antibody (ab49343)

ab49343 staining mouse embryonic brain slice tissue sections by IHC-Fr. Tissue sections were fixed with paraformaldehyde and permeabilized with 0.1% Triton-X in 0.1M PBS. The sample was blocked with 5% serum for 2 hours at 4°C prior to incubation with the primary antibody, diluted 1/20 in 0.1M PBS for 24 hours at 4°C. An Alexa Fluor® 546 conjugated goat anti-rabbit IgG antibody was used as the secondary.
This image is courtesy of an anonymous Abreview
Immunocytochemistry/ Immunofluorescence-Non Neuronal Enolase antibody(ab49343)

ICC/IF image of ab49343 stained MCF7 cells. The cells were 100% methanol fixed (5 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab49343, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
This product has been referenced in:
See all 3 publications for this product
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Anti-Non Neuronal Enolase antibody (ab49343) at 0.03 µg/ml + Fetal intestine lysate 10µg
Secondary
HRP conjugated anti-Rabbit IgG at 1/50000 dilution
Predicted band size : 47 kDa
Observed band size : 47 kDa

ab49343 at 4µg/ml staining Non Neuronal Enolase in epithelial cells of collecting tubules (arrows) of human kidney tissue.

ab49343 staining mouse embryonic brain slice tissue sections by IHC-Fr. Tissue sections were fixed with paraformaldehyde and permeabilized with 0.1% Triton-X in 0.1M PBS. The sample was blocked with 5% serum for 2 hours at 4°C prior to incubation with the primary antibody, diluted 1/20 in 0.1M PBS for 24 hours at 4°C. An Alexa Fluor® 546 conjugated goat anti-rabbit IgG antibody was used as the secondary.
This image is courtesy of an anonymous Abreview

ICC/IF image of ab49343 stained MCF7 cells. The cells were 100% methanol fixed (5 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab49343, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
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