Location:Home > Recombinant antibody

Anti-turboGFP, AlpSdAbs® VHH(Biotin)

Details and Advantages
Applications: ELISA,Purification
Reactivity: turboGFP
Conjugate: Biotin
Advantages:

High lot-to-lot consistency

Increased sensitivity and higher affinity

Animal-free production

Summary >

Description: 

Anti-turboGFP, AlpSdAbs® VHH(Biotin) is designed for detecting turboGFP fusion proteins. Anti-turboGFP, AlpSdAbs® VHH(Biotin) is based on monoclonal, recombinant, single domain antibody to turboGFP coupled to Biotin, and Anti-turboGFP, AlpSdAbs® VHH(Biotin) detects the turboGFP selectively, no reactivity with other proteins.


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

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

IP:         1-2ug/sample

BLI (biolayer interferometry)

SPR (surface plasmon resonance)


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.