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

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

High lot-to-lot consistency

Increased sensitivity and higher affinity

Summary >

Description:
Anti-Camel IgG(H+L), AlpHcAbs® Goat antibody(HRP) is designed for detecting Camel IgG(H+L) specifically. Based on immunoelectrophoresis and/or ELISA, Anti-Camel IgG(H+L), AlpHcAbs® Goat antibody(HRP) reacts with Camel IgG heavy chain and light chain selectively.

Immunogen: Camelus dromedarius immunoglobulins                  
Host: Goat
Isotype: Goat IgG
Conjugate:  HRP
Specificity: Camel IgG(H+L)
Cross-Reactivity: Camel IgG and with light chains common to other Camel immunoglobulins(such as IgA,IgM). No was detected against non-immunoglobulin serum proteins. The antibody may cross-react with immunoglobulins from other species.
Purity: 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:
The biological family Camelidae comprises camels (one-humped Camelus dromedarius and two-humped Camelus bactrianus), llama (Lama glama and Lama guanicoe), and vicugna (Vicugna vicugna and Vicugna pacos). Camelidae contain two kinds of IgG in serum: conventional antibodies (IgG1) containing two light chains and two heavy chains (composed of the VH, CH1, hinge, and CH2 and CH3 domains) and two types of homodimeric heavy-chain antibodies (HCAbs), IgG2 and IgG3, which comprise only H chains; each H chain contains a VHH, hinge, and CH2 and CH3 domains. The smallest intact functional antigen-binding fragment of HCAbs is the single-domain VHH, also known as a nanobody(Nb).

Performance >

WB:                1:5000-1:50000
ELISA:            1:10000-1:50000
IHC:               1:200 - 1:5000
IHC-Paraffin: 1:200-1:5000
Almost it can be used for VHH that come from Camel

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.