1 gainst carbonic anhydrase II, H+ -ATPase and Band 3 protein.

2  sections using antibodies to H+ -ATPase and Band 3 protein.

3 ed large-scale conformational changes in the band 3 protein.

4  charged groups of the cytoplasmic domain of Band 3 protein also produce an allosteric effect on S-ni

5 the cytoplasmic portion of red cell membrane Band 3 protein and its corresponding N-terminal 11-resid

6 ports the hypothesis that cryptic regions of band 3 protein are parasite-induced, host-derived erythr

7 imentally measured diffusion coefficients of band-3 proteins are higher in elliptocytes than in spher

8      Formation and deoxygenation of a SNO-Hb/Band 3 protein assembly does not in itself cause NO rele

9 s variant suggests that expression of mutant band 3 protein can be rescued by wild-type band 3.

10          Other studies show that some mutant band 3 protein can mediate a cation conductance.

11                                          The band 3 proteins function as anion transporters, acid bas

12 n of mutant band 3 RNA and the deficiency of band 3 protein in this kindred.

13 ined by an allelic change (Lys658Glu) in the band 3 protein; nevertheless, the Wrb antigen apparently

14 imate the macroscopic diffusion constant for band 3 protein on the surface of human erythrocytes.

15  microscopy techniques show that NBD-lipids, band 3 protein, protein 4.1, ankyrin, and spectrin are a

16 m the second (M12) methionine codon and that band 3 protein represented a U(L)13-independent, posttra

17 f the transport site of human red blood cell band 3 protein under various conditions by analyzing the

18             Colocalization of H+ -ATPase and Band 3 protein was performed by double labeling using an

19 nd cytoplasmic H+-ATPase, but no basolateral Band 3 protein, was observed exclusively in the CNT and