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|Tested species reactivity||Human|
|Host / Isotype||Rabbit / IgG|
|Immunogen||Synthetic peptide corresponding to the C-terminal portion of human NSE.|
|Purification||Antigen affinity chromatography|
|Storage buffer||PBS, pH 7.4, with 1% BSA|
|Contains||0.09% sodium azide|
|Storage Conditions||4° C, do not freeze|
|Tested Applications||Dilution *|
|Immunohistochemistry (Paraffin) (IHC (P))||1:300|
* Suggested working dilutions are given as a guide only. It is recommended that the user titrate the product for use in their own experiment using appropriate negative and positive controls.
PA1-21081 detects NSE in Human samples.
PA1-21081 has been successfully used in immunohistochemistry (FFPE) procedures. Formalin-fixed paraffin-embedded tissue sections require boiling in 10 mM citrate buffer (pH 6.0) prior to immunostaining.
The PA1-21081 immunogen is a synthetic peptide corresponding to the C-terminal portion of human NSE.
Enolase is a glycolytic enzyme catalyzing the reaction pathway between 2-phospho-glycerate and phosphoenol pyruvate. In mammals, enolase molecules are dimers composed of three distinct subunits (alpha, beta and gamma). The alpha subunit is expressed in most tissues and the beta subunit only in muscle. The gamma subunit is expressed primarily in neurons, in normal and in neoplastic neuroendocrine cells. Coexpression of NSE (neuron specific enolase) and chromogranin A is common in neuroendocrine neoplasms.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
2-phospho-D-glycerate hydro-lyase; 2-phospho-D-glycerate hydrolyase; Eno; ENOG; enolase 2 (gamma, neuronal); epididymis secretory protein Li 279; glycerate hydrolyase; Neural Enolase; Neuron Specific Enolase; neuron specific gamma enolase; neuron-specific enolase; Neuronal Enolase; neuronal enriched enolase; neurone-specific enolase
ENO2; HEL-S-279; NSE