Anti-mNeogreen, AlpSdAbs® VHH(HRP)

Details and Advantages

                                                Applications:
                                                WB,ELISA
                                            
                                                Reactivity:
                                                mNeongreen
                                            
                                                Conjugate:
                                                HRP
                                            
                                                Advantages:
                                                High lot-to-lot consistency
Increased sensitivity and higher affinity
Animal-free production

概述 >

Description:

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

Immunogen: mNeongreen
Host: Alpaca pacous
Isotype: VHH domain of alpaca IgG2b/2c
Conjugate: HRP
Specificity: mNeongreen
Cross-Reactivity: Highly selective for mNeongreen
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
Storage: Store at –20 °C(Avoid freeze / thaw cycles)

Background:

mNeongreen is the brightest monomeric green or yellow fluorescent protein yet described to our knowledge, performs exceptionally well as a fusion tag for traditional imaging as well as stochastic single molecule super-resolution imaging and is an excellent fluorescence resonance energy transfer(FRET) acceptor for the newest cyan fluorescent proteins.

性能 >

WB: 1:1,000-1:5000
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.