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应用
来自荆豆（gorse, furze）的凝集素已被用于：
- 免疫组化中作为的潘氏细胞标记物（稀释度为 1:1,000 ）
- 血管定量中内皮细胞双重染色
- 支气管上皮细胞的组化染色
生化/生理作用
荆豆凝集素具有抗H血型特异性。凝集素有两种类型： UEA I 对 L-岩藻糖具有亲和力，而 UEA II 对 N,N′-二乙酰壳二糖具有亲和力。最初认为UEA I摩尔量为170,000道尔顿。 后来的报道表明，UEA I可以在中性和碱性pH下形成聚集体，正确的摩尔量是68,000道尔顿。
包装
包装尺寸基于蛋白质含量。
联系
由亲和纯化的凝集素制备缀合物。
外形
含有柠檬酸钠
分析说明
凝集活性以μg/ml表示，由磷酸盐缓冲盐水（pH 6.8）连续稀释1 mg/ml溶液而测得。该活性是指25℃孵育1小时后使2％人O型血红细胞悬浮液凝集的最低浓度。
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
法规信息
动植物源性产品
常规特殊物品
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
Heather Ireland et al.
Developmental dynamics : an official publication of the American Association of Anatomists, 233(4), 1332-1336 (2005-06-07)
Here, we exploit an absolute differential between stem and progeny cells in their ability to express Cre from a somatically inducible transgene to determine the longevity of intestinal Paneth cells. In the Ahcre transgenic line induction of Cre recombinase allows
Daisuke Kondoh et al.
Cells, tissues, organs, 203(1), 20-28 (2016-07-18)
Glycoconjugates in the olfactory system play critical roles in neuronal formation, and α1-2 fucose (α1-2Fuc) glycan mediates neurite outgrowth and synaptic plasticity. Histochemical findings of α1-2Fuc glycan in the mouse olfactory system detected using Ulex europaeus agglutinin-I (UEA-I) vary. This
Maria Hernandez et al.
Biomedicines, 9(11) (2021-11-28)
The purpose of this study was to assess vascular and histological alterations in two COVID-19 and three control post-mortem retinas. The macular areas of flat-mounted samples were processed for immunofluorescence. Lectin and collagen IV positive vessels were captured under confocal
M Tango et al.
Archives of histology and cytology, 63(1), 81-89 (2000-04-19)
The aggregation of lymphoid cells in the bronchial mucosa has been named the bronchus-associated lymphoid tissue (BALT) and investigated in comparison with the gut-associated lymphoid tissue (GALT). To elucidate precisely the structure and function of the BALT, the present study
Sarah Waters et al.
Acta neuropathologica communications, 9(1), 144-144 (2021-08-28)
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease involving progressive degeneration of upper and lower motor neurons. The pattern of lower motor neuron loss along the spinal cord follows the pattern of deposition of phosphorylated TDP-43 aggregates. The blood-spinal
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