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Antikörper

Recombinant NSE Monoclonal Antibody

Produktgrößen
50 ul
£281,00
AN301611L-50UL
100 ul
£402,00
AN301611L-100UL
Über dieses Produkt
SKU:
AN301611L
Zusätzliche Namen:
ENO,HEL-S,enolase,ENO2,HEL-S-279,NSE,enolase 2,2-phospho-D-glycerate hydro-lyase,Enolase G Gamma,Gamma-enolase,ENOG,Neural enolase,Neuron-specific enolase,2 phospho D glycerate hydrolyase,Eno 2,Enolase 2 (gamma,Enolase 2 gamma neuronal,Enolase2,Epididymis secretory protein Li 279,Gamma enolase,HEL S 279,Neuron specific enolase,Neuron specific gamma enolase,neuronal enriched enolase,neuronal),Neurone specific enolase,Neuron-specific enolase (NSE)
Anwendung:
Flow Cytometry, Immunofluorescence, Immunoprecipitation, Western Blot
Buffer:
PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant.
translate.label.attr.clone:
A314
Klonalität:
Recombinant Monoclonal
Konzentration:
1 mg/ml
Weitere Details:
Has neurotrophic and neuroprotective properties on a broad spectrum of central nervous system (CNS) neurons. Binds, in a calcium-dependent manner, to cultured neocortical neurons and promotes cell survival.
Host:
Rabbit
Immunogen:
Recombinant human NSE fragment
Isotyp:
IgG, kappa
Aufreinigung:
Protein A Purified
Reaktivitäten:
Human, Mouse, Rat
Versandbedingungen:
Blue Ice
Lagerbedingungen:
-20[o]C Avoid freeze/thaw cycles.
Hersteller:
Elabscience
Typ:
Antibody: Recombinant Antibodies
Western Blot with NSE Monoclonal Antibody at dilution of 1:2000. Lane 1: HeLa, Lane 2: SH-SY5Y, Lane 3: U87-MG, Lane 4: Mouse brain, Lane 5: Rat brain
Immunofluorescent analysis of (4% Paraformaldehyde) fixed HeLa cells using anti-NSE Monoclonal Antibody at dilution of 1:100.
Immunofluorescent analysis of (4% Paraformaldehyde) fixed Ramos cells using anti-NSE Monoclonal Antibody at dilution of 1:200.
Immunofluorescent analysis of (4% Paraformaldehyde) fixed NIH/3T3 cells using anti-NSE Monoclonal Antibody at dilution of 1:50.
Flow cytometric analysis of human NSE expression on HeLa cells. Cells were stained with purified anti-Human NSE, then a Alexa Fluor 488-conjugated second step antibody. The histogram were derived from events with the forward and side light-scatter characteristics of intact cells.