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=1723202232&Signature=0On3Z1hBTKUObBuBBMRUkknKvyaQ82nmHoDobyCkfW5Whiy9OB9asxinHC5C-w~FEb~34JcQGvMjvb1H89uQUxli-5DGSDGW1ILlXnghg2v1ef3yEglUpO4OxbMB~IVxcqX2IWnuf0Rh7fLK9J23RPsbmWPsB7U4ZVCqmFp6qfIA0TFRAdWCEcx97j~djtjgg951vNGmnAHik9x3FGd6iA1Fmqs0UO5u6q0fIQNtA7lzKzkg5KonL-lEfZBmEARoviPEWoxzKKtJm48Ma~XFh0ezDL56Nh6zARKLy4oy-o2LqSFh9nDbfss68Fq52aWzSCO5UcQ6NtWLhBs2Lruwtw__&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.”
