Anti-IgG1 Fc [TP1107]

Catalogue Number: AB01436-23.9-BT-ABA

Manufacturer:Vector Laboratories, Inc (ABA)
Type:Monoclonal Secondary Antibody - Unconjugated
Alias:immunoglobulin G1 fragment crystallizable region; immunoglobulin G1 Fc region; immunoglobulin G1
Shipping Condition:Blue Ice
Unit(s): 1 mg
Host name: Rabbit
Clone: TP1107
Isotype: IgG
Immunogen: This antibody was raised by immunising alpacas with 1.0 mg polyclonal mouse IgG. Subsequently, the generation of nanobody immune libraries and the selection of antigen-specific nanobodies by phage display from these libraries were performed.
Application: ICC, IF, WB, DB

Additional Text

Purification

Purified

Antibody Clonality

Recombinant Monoclonal

Storage Note

Store at 4⁰C for up to 3 months. Note, this antibody is provided without added preservatives, it is therefore recommed this antibody be handled under sterile conditions. For longer storage, aliquot and store at -20⁰C.

Application Notes

Anti-IgG nanobodies can often perform more efficiently than polyclonal secondary antibodies in various experimental assays. For instance, this nanobody conjugated with a maleimide-activated HRP was used to detect mouse IgG1 via ECL Western blot and it considerably outperformed a polyclonal secondary antibody-HRP conjugate (Pleiner et al., 2018). Similarly, this nanobody conjugated with the infrared fluorophore IRDye 800 performed equally or better than a polyclonal anti-mouse IgG secondary antibody in Western blotting on HeLa cell lysate (Pleiner et al., 2018). TP1107 nanobody can also be used as an efficient high-affinity reagent for immunofluorescence. It was utilised in conjugation with two to three fluorophores in detection of mouse monoclonal IgG1 for the indirect immunostaining of HeLa cells where it performed exceptionally well as for a non-polyclonal antibody reaching similar signal strength to polyclonal agents when it was combined with another anti-IgG1 nanobody (Pleiner et al., 2018). Monovalent nanobodies can be also effectively used in a single step immunostaining procedure because they do not create large, cross-linked complexes with primary antibodies. TP1107 was used as a secondary reagent; it was first incubated with a primary antibody and then a one-step immunostaining was performed (without the usual separate incubation with a primary and secondary antibody) (Pleiner et al., 2018).

Short Description

This chimeric rabbit antibody was made using a variable domain sequence of the original VHH format, for improved compatibility with existing reagents, assays and techniques.