TRIP230/TRIP11 antibody | knockout validation | LifeSpan Biosciences LS-C20059

This is a knockout-validated antibody summary, based on the publication "The skeletal phenotype of achondrogenesis type 1A is caused exclusively by cartilage defects", as cited below [1]. Labome curates formal publications to compile a list of antibodies with unambiguous specificity within Validated Antibody Database (VAD).

TRIP230/TRIP11 antibody | knockout validation | LifeSpan Biosciences LS-C20059 figure 1
Figure 1. Western blot with a GMAP-210-specific antibody on the cell lysates of mouse embryonic fibroblasts extracted from E13.5 wild-type, Trip11−/+ and knockout embryos. Note the complete absence of GMAP-210 protein in the knockout (−/−) cell lysate. From [1].
Antibody information

Mouse monoclonal IgG1

Company: LifeSpan Biosciences

Antibody: TRIP230/TRIP11

Catalog number: LS-C20059

Summary: Mouse monoclonal IgG1 against recombinant human TRIP230/TRIP11 (GMAP-210)(epitope: aa 1099-1372). Reacts with human by western blot and immunoprecipitation. Not suitable for immunohistochemistry (paraffin).

Validation Method

Western blot

Sample

Mouse embryonic fibroblasts extracted from E13.5 wild-type, Trip11−/+ and knockout embryos. Cells were lysed on ice in 1 ml mammalian lysis buffer (Promega) containing 1× protease inhibitor cocktail (Promega) for 10 min.

Blocking agent

Western breeze blocking buffer (Life Technologies) for 30 min.

Primary incubation

1/500 dilution in western breeze antibody dilution buffer for 1 h at room temperature.

Secondary incubation

1/10,000 dilution peroxidase-coupled goat anti-mouse IgG (Thermo Scientific, 31320) in western breeze antibody dilution buffer for 1 h at room temperature.

Detection

for 5 min with Tropix CDP star substrate (Applied Biosystems). Immunoreactive bands were visualized using Hyblot CL autoradiography film (Denville).

Clone note

The same clone (10G5) is sold as LifeSpan Biosciences LS-C20059; Invitrogen MA1-23294.

References
  1. Bird I, Kim S, Schweppe D, Caetano Lopes J, Robling A, Charles J, et al. The skeletal phenotype of achondrogenesis type 1A is caused exclusively by cartilage defects.. Development. 2018;145: pubmed publisher