Fig. 1.
Fig. 1. Construction of deletion-type c-kit cDNA. (A) Schematic representation of deletion-type KIT. Location of signal peptide (SP), transmembrane (TM), and tyrosine residue of autophosphorylation (Y) are indicated. KITTyr814 and KITDel-Tyr814 carries a point mutation (Asp to Tyr) in codon 814. (B) Expression of KITDel-Wild and KITDel-Tyr814. 293T cells were transfected with c-kitDel-Wild and c-kitDel-Tyr814 cDNA, and then cells were labeled for 5 hours with [35S]-methionine and lysed. KIT was immunoprecipitated with ACK2 MoAb (ECD), rabbit anti-KITKinase serum (Kinase), and rabbit anti-KITC-terminal serum (C-terminal) and analyzed by SDS-PAGE and autoradiography. The similar results were obtained from three independent experiments.

Construction of deletion-type c-kit cDNA. (A) Schematic representation of deletion-type KIT. Location of signal peptide (SP), transmembrane (TM), and tyrosine residue of autophosphorylation (Y) are indicated. KITTyr814 and KITDel-Tyr814 carries a point mutation (Asp to Tyr) in codon 814. (B) Expression of KITDel-Wild and KITDel-Tyr814. 293T cells were transfected with c-kitDel-Wild and c-kitDel-Tyr814 cDNA, and then cells were labeled for 5 hours with [35S]-methionine and lysed. KIT was immunoprecipitated with ACK2 MoAb (ECD), rabbit anti-KITKinase serum (Kinase), and rabbit anti-KITC-terminal serum (C-terminal) and analyzed by SDS-PAGE and autoradiography. The similar results were obtained from three independent experiments.

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