ライフサイエンスコーパス: plant lectin

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1 n of internal alpha1,3-glucosidic bonds by a plant lectin.

2 s in the binding properties toward different plant lectins.

3 amster ovary (CHO) cell mutants resistant to plant lectins.

4 tin-1, its two mutants, and the Gal-specific plant lectins.

5 The glycans were interrogated using plant lectins and antibodies in sera from mice infected

6 these findings for possible in vivo roles of plant lectins and for the use of concanavalin A as a res

7 cell surface glycoconjugates recognized by a plant lectin are selectively associated with these "reti

8 Overall, we find that conjugated plant lectins are effective tools for combinatory bioche

9 influenza virus hemagglutinins, siglecs, and plant lectins are largely unaffected by adjacent interna

10 Plant lectins are useful targets for biophysical studies

11 In addition, the plant lectin Bandeiraea simplicifolia-I was employed to

12 Unlike other plant lectins, both DGL and ConA bind with high affinity

13 Our studies demonstrate that a plant lectin can serve as a transneuronal tracer when it

14 the selective binding of the polymers to the plant lectin concanavalin A.

15 sugar-binding protein receptors such as the plant lectins concanavalin A and the highly toxic mistle

16 weakly charged molecule, by displacement of plant lectin (concavalin A) bound to a polysaccharide (d

17 with concanavalin A (ConA), a member of the plant lectin family.

18 Plant lectins have been implicated as playing an importa

19 re defined by cell body size, binding of the plant lectin IB(4) and responsiveness to the algogenic c

20 The new array was first tested with several plant lectins, including concanavalin A (conA), Vicia vi

21 from primary sensory afferents that bind the plant lectin isolectin B4 (IB4).

22 tudy demonstrated that the O-glycan-specific plant lectin jacalin binds Dsg1 and inhibits the interac

23 mass spectroscopy and FACS analysis with the plant lectin l-phytohemagglutinin.

24 Some plant lectins like Griffonia simplicifolia lectin I and

25 ns, via fusion to a second protein such as a plant lectin or a luteovirus coat protein for transcytos

26 Interestingly, another plant lectin, peanut agglutinin, which shares the same c

27 Similar to plant lectins, pertussis toxin (PTx) can activate the TC

28 LR4 was activated by a non-LPS stimulus, the plant lectin PHA.

29 anterograde axonal tracing method using the plant lectin Phaseolus vulgaris leucoagglutinin (PHA-L)

30 Although it has been proposed that plant lectins play a number of roles, the function of th

31 Gal-1 and the plant lectins possess essentially the same affinities fo

32 Here we investigate the plant lectin RTB as a novel carrier for human lysosomal

33 ttern of binding of two sialic acid-specific plant lectins, Sambucus nigra agglutinin and Maackia amu

34 Plant lectins such as phytohemagluttinin (PHA) can activ

35 This contrasts with galectin-1 and many plant lectins that form homogeneous, organized cross-lin

36 easibility of high throughput screening with plant lectins to identify compounds that alter muscle ce

37 ed the spatial distribution of two different plant lectins, Ulex europaeus agglutinin (UEA) and Dolic

38 In contrast, the plant lectin vicia villosa-B4 (VVL-B4), which shares the

39 ster ovary cells and four galactose-specific plant lectins were investigated by isothermal titration

40 urpurea agglutinin, a Gal and GalNAc binding plant lectin, were isolated from 17 strains by anion exc

41 We used high throughput screening with the plant lectin Wisteria floribunda agglutinin (WFA) to ide

42 n, a naturally occurring, galactose-specific plant lectin with extremely potent shiga toxin-like enzy

43 riments using succinylated concanavalin A, a plant lectin with high affinity for mannose, revealed th

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