ライフサイエンスコーパス: peanut agglutinin

1 CT (57%) and GL7 (52%), and bound the lectin peanut agglutinin.

2 calized via the binding of cholera toxin and peanut agglutinin.

3 fibronectin, U. europaeus, R. communis, and peanut agglutinin.

4 d by binding to Vicia villosa agglutinin and peanut agglutinin.

5 We demonstrate that peanut agglutinin, a minor peanut allergen, is a novel l

6 Peanut agglutinin activates DCs to induce the expression

7 Immunohistochemical analyses with peanut agglutinin and an antibody specific for cone tran

8 ctural integrity was determined by IHC using peanut agglutinin and an M-opsin-specific antibody.

9 these pulmonary lymphoid aggregates express peanut agglutinin and GL7, two markers of GC B cells, as

10 Binding affinities to peanut agglutinin and human galectin-3 were measured by

11 ase diminished alpha-dystroglycan binding to peanut agglutinin and inhibited neuraminidase-induced AC

12 lfate proteoglycan core protein, which binds peanut agglutinin and is localized to the interphotorece

13 aterial, positive for binding of the lectin, peanut agglutinin, and an antibody to the carbohydrate e

14 of surface IgD, a high level of receptor for peanut agglutinin, and expression of mutated antibody V

15 e uptake of biocytin, labeled the cones with peanut agglutinin, and then used antibodies against blue

16 ing of primary tumors showed the presence of peanut agglutinin binding (PNA(+)) highly mitotic lympho

17 and matrix sheets, IRBP colocalized with the peanut agglutinin binding matrix glycans.

18 itrophenyl)acetyl-Ficoll induces clusters of peanut agglutinin-binding B cells in the spleen.

19 g for molecules of the extracellular matrix (peanut agglutinin-binding components, tenascin, chondroi

20 ognized by the lectins Datura stramonium and peanut agglutinin (by approximately 74 and approximately

21 ribution of IRBP, as well as glycans binding peanut agglutinin (cone matrix) and wheat germ agglutini

22 gic stains as well as cell-specific markers (peanut agglutinin for cone photoreceptors and calbindin

23 ium iodide, for NTs and rhodamine-conjugated peanut agglutinin for synaptic ECM.

24 ient mice demonstrated a diminished level of peanut agglutinin+ germinal centers and a failure in iso

25 rchitecture (cresyl violet), histochemistry (peanut agglutinin), immunocytochemistry (antibodies to a

26 sin, rod alpha-transducin, and S-antigen and peanut agglutinin labeling for cone interphotoreceptor m

27 terphotoreceptor-binding protein (IRBP), and peanut agglutinin lectin (PNA).

28 Like jacalin, peanut agglutinin lectin also binds the core 1 disacchar

29 Peanut agglutinin lectin binding studies revealed a mosa

30 cosyl Yariv reagent but interacting with the peanut agglutinin lectin was proposed.

31 ncreased CD31 binding to Arachis hypogaea or peanut agglutinin lectin, indicating CD31 desialylation.

32 cell surface detected by enhanced binding of peanut agglutinin lectin.

33 ion as detected by staining with jacalin and peanut agglutinin lectins after 30 min of treatment; no

34 Blotting with Maackia amurensis and peanut agglutinin lectins established epidermal growth f

35 y mutated in B220+ splenic B cells with high peanut agglutinin levels at a frequency similar to that

36 d or immunized splenic B220+ cells with high peanut agglutinin levels.

37 show that C2C12 alpha-dystroglycan bound to peanut agglutinin only after digestion with neuraminidas

38 ling of their inner segments with the lectin peanut agglutinin or by colabeling with antisera to cone

39 rating, they express germinal center markers peanut agglutinin or CD10 but not Bcl-6, and most expres

40 However, profiles did vary with peanut agglutinin, Phaseolus vulgaris leucoagglutinin, S

41 lated with the presence of binding sites for peanut agglutinin (PNA) [specific for Gal beta (1-3) Gal

42 The lectin peanut agglutinin (PNA) and antibodies to short (S)- and

43 Binding kinetics of the multivalent proteins peanut agglutinin (PnA) and cholera toxin B subunit (CTB

44 A galactose-binding peanut agglutinin (PNA) and sialic acid-binding Sambucus

45 ascin, chondroitin sulfate proteoglycan, and peanut agglutinin (PNA) binding sites--were investigated

46 creatic cell types, and found that UEA-I and Peanut agglutinin (PNA) have a specific affinity for aci

47 Cone photoreceptors were stained by peanut agglutinin (PNA) lectin in the flatmounted retina

48 na sections with the anti-RPE65 antibody and peanut agglutinin (PNA) lectin, which is known to label

49 retinaldehyde-binding protein (CRALBP), and peanut agglutinin (PNA) lectin.

50 ced and the area of the future IVD contained peanut agglutinin (PNA) staining cartilage.

51 ompetes with TF-antigen for binding sites on peanut agglutinin (PNA) that is immobilized on magnetic

52 binding-enhancing effect of beta-Lact toward peanut agglutinin (PNA), a lectin strongly binding multi

53 products showed positive lectin staining by peanut agglutinin (PNA), Maclura pomifera agglutinin (MP

54 xhibit a characteristic increased binding of peanut agglutinin (PNA), reflecting an increased express

55 Flow cytometry sorted peanut agglutinin (PNA)-labeled cones from dissociated m

56 be enriched by their affinity for the lectin peanut agglutinin (PNA).

57 e examined remained intact and positive with peanut agglutinin (PNA).

58 eased binding by the mAb 1B11 and the lectin peanut agglutinin (PNA).

59 llary acidic protein (GFAP) and biotinylated peanut agglutinin (PNA).

60 th these viruses showed increased binding to peanut agglutinin (PNA).

61 recognized by the galactose-specific lectin peanut agglutinin (PNA).

62 een, they both developed GC-like clusters of peanut agglutinin-positive (PNA+) cells in their LNs.

63 postimmunization, when they were evident in peanut agglutinin-positive germinal center B cells.

64 LT.LT alpha-/- mice had germinal center-like peanut agglutinin-positive regions, but lacked follicula

65 enters (GC), where mouse B cells up-regulate peanut agglutinin receptor (PNA-R), B7-2 (CD86), and MHC

66 ns Ulex europaeus, Bandeiraea simplicifolia, peanut agglutinin, Ricinis communis, and wheat germ aggl

67 Confocal microscopy of peanut agglutinin-stained sections showed dose-dependent

68 Cone density was assessed by peanut agglutinin staining and confocal microscopy.

69 Cone morphology was assessed by peanut agglutinin staining in retinal flatmounts and cry

70 sis that followed a reduction in jacalin and peanut agglutinin staining.

71 n Irbp(-/-) retina, and was colocalized with peanut agglutinin to the Irbp(-/-) cone outer segments.

72 The number of cones labeled by peanut agglutinin was decreased 50-60%.

73 II, succinylated wheat germ agglutinin, and peanut agglutinin were significantly increased in the lu

74 e system using the lectins Helix aspersa and peanut agglutinin, which bind to alternative forms of O-

75 Interestingly, another plant lectin, peanut agglutinin, which shares the same carbohydrate sp