Fig. 2.
![Fig. 2. Association of mutant [674R]GPIIb with the endoplasmic reticulum chaperone BiP. / CHO cells were transiently transfected with the indicated cDNAs, lysed, and immunoprecipitated with the anti-GPIIb moAb M3. The precipitates were resolved by electrophoresis, transferred to nitrocellulose membrane, and blotted with polyclonal anti-BiP antibody, as described in “Materials and methods.”](https://ash.silverchair-cdn.com/ash/content_public/journal/blood/97/9/10.1182_blood.v97.9.2640/6/h80910985002.jpeg?Expires=1735832440&Signature=T7pinj8wJABAtffsY4myat8HEi5A50EGoUTG8lpnB6zp2yO4D12jCWDc7MQaIaOc4zAp9dbezeel98~CM8CRgJh-MfWUcVWjAt6HtxLWse9xhTtrNfuJ~Bbw4jQPFAx~F9NHnyq6J00ayrGTAZ9C4KAM7pZgQDB6Siag4myi0lns4muKZhv8DIBquZ8TX7i55NZ2ErJU76zArMcFapzRVc81Uo4eJTzeTjJTOqy9CNkmr7pqKk0y4fDi1VAXrv~tYcK7F2Vr9UJLnvtRSrDP5zHMsJ3HwAfOfD1tg1Qm~tLbPJQOHpiokOv3NN86FFAt2-QVgKqeQD9lz6ItjYwWEg__&Key-Pair-Id=APKAIE5G5CRDK6RD3PGA)
Association of mutant [674R]GPIIb with the endoplasmic reticulum chaperone BiP.
CHO cells were transiently transfected with the indicated cDNAs, lysed, and immunoprecipitated with the anti-GPIIb moAb M3. The precipitates were resolved by electrophoresis, transferred to nitrocellulose membrane, and blotted with polyclonal anti-BiP antibody, as described in “Materials and methods.”
