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Anti-Rabbit IgG(H+L), AlpHcAbs® Goat antibody(HRP)

Details and Advantages
Applications: WB,ELISA
Reactivity: Rabbit IgG(H+L)
Conjugate: HRP
Advantages:

High lot-to-lot consistency

Increased sensitivity and higher affinity

Animal-free production

Summary >

Description:
Anti-Rabbit IgG(H+L), AlpHcAbs® Goat antibody(HRP) is designed for detecting rabbit IgG(H+L) specifically. Anti-Rabbit IgG(H+L), AlpHcAbs® Goat antibody(HRP) is based on monoclonal, recombinant, goat IgG Fc fused single domain antibody to rabbit IgG(H+L) coupled to HRP. Based on immunoelectrophoresis and/or ELISA, Anti-Rabbit IgG(H+L), AlpHcAbs® Goat antibody(HRP) reacts with rabbit IgG(H+L) selectively, no reactivity with mouse, human, cynomolgus, rat, goat IgG.

Immunogen: Recombinant Rabbit IgG                  
Host: Alpaca pacous
Isotype: VHH domain of alpaca IgG2b/2c fused to goat IgG Fc(mutation)    
Conjugate:  HRP
Specificity: Rabbit IgG(H+L)
Cross-Reactivity: No cross-reactivity with mouse, human, cynomolgus, rat, goat IgG    
Purity: Recombinant Expression and Affinity purified
Concentration: 1mg/ml
Formation: Liquid, 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, Stable for 12 months at -20°C

Background:
Rabbit research antibodies are widely used in life science research. So far, four isotypes have been identified (IgA, IgE, IgG, and IgM) in rabbits. Each isotype has a different heavy chain. Rabbit has only one IgG subclass. The whole IgG molecule possesses both the Fc region and the Fab region, which possessing the epitope-recognition site. The IgG contains two heavy and light chains. The heavy chain is about 50 KD and the light chain is about 25 KD. The common IgG is monomeric with a molecular weight of approximately 150 kD.
Using antibody with Fc(mutation), the background from Fc receptors will be eliminated.

Performance >


ELISA:   1:10000-1:50000
WB:      1:10000-1:50000


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.