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Anti-turboGFP, AlpHcAbs® Rabbit antibody(HRP)

Details and Advantages
Applications: WB,ELISA
Reactivity: turboGFP
Conjugate: HRP
Advantages:

High lot-to-lot consistency

Increased sensitivity and higher affinity

Animal-free production

Summary >

Description: 

Anti-turboGFP, AlpHcAbs® Rabbit antibody(HRP) is designed for detecting turboGFP fusion proteins specifically. Anti-turboGFP, AlpHcAbs® Rabbit antibody(HRP) is based on monoclonal, recombinant, rabbit Fc fused single domain antibody to turboGFP coupled to HRP, and the Anti-turboGFP, AlpHcAbs® Rabbit antibody(HRP) detects turboGFP fusion proteins selectively, no reactivity with other proteins.

Immunogen: TurboGFP
Host: Alpaca pacous
Isotype: VHH domain of alpaca IgG2b/2c fused to Rabbit IgG Fc    
Conjugate: HRP
Specificity: TurboGFP
Cross-Reactivity: No cross-reactivity with CopGFP, jellyfish GFP and derivatives
Affinity: Dissociation constant KD of 0.1nM      
Purity: Recombinant Expression and Affinity purified
Concentration: 1mg/ml
Buffer: 10mM PBS (pH 7.5), 0.05% sucrose, 0.1% trehalose, 0.01% proclin300,50% Glycerol
Storage: Store at –20 °C(Avoid freeze / thaw cycles), protect from light,


Background:

The dimeric green fluorescent protein TurboGFP is derived from the green fluorescent protein CopGFP of the copepod Pontellina plumata. It possesses bright green fluorescence with excitation maximum at 482 nm and emission maximum at 502 nm. TurboGFP is a fast maturating protein: its fluorescent signal is visible earlier than other green fluorescent proteins. TurboGFP shares only about 20% sequence identity with jellyfish GFP variants. Therefore, most anti-GFP antibodies do not bind to TurboGFP. TurboGFP is mainly intended for applications where fast appearance of bright fluorescence is crucial. It is specially recommended for cell and organelle labeling and tracking the promoter activity. Destabilized TurboGFP variant allows accurate analysis of rapid and/or transient events in gene regulation.




Performance >


ELISA:   1:5,000-1:20000


Dilution factors are presented in the form of a range because the optimal dilution is a function of many factors, such as antigen density, permeability, etc. The actual dilution used must be determined empirically.