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L1394

Sigma-Aldrich

来自 普通小麦 的凝集素（小麦）

agarose conjugate, saline suspension

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别名:
WGA, Wheat germ agglutinin
NACRES:
NA.32

偶联物

agarose conjugate

质量水平

200

形式

saline suspension

标记范围

~6 mg per mL

基质

4% agarose

基质活化

cyanogen bromide

基质隔离区

1 atom

粒径

45-165 μm

容量

≥0.5 mg/mL binding capacity (ovomucoid)

储存温度

2-8°C

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相关类别

应用

用于纯化含有（D-N-乙酰氨基葡萄糖）2或N-乙酰神经氨酸的糖蛋白。

生化/生理作用

WGA 不具有血型特异性，但具有与 N-乙酰基-β-D-葡糖胺残基和 N-乙酰基-β-D-葡糖胺低聚物的亲和性。WGA 不含蛋白结合糖。

外形

含15 mM叠氮化钠的0.9% NaCl中的混悬剂。

制备说明

由亲和纯化凝集素制备偶联物。

储存分类代码

10 - Combustible liquids

WGK

WGK 3

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Bo F Hansen et al.
PloS one, 7(5), e34274-e34274 (2012-05-17)
There is controversy with respect to molecular characteristics of insulin analogues. We report a series of experiments forming a comprehensive characterisation of the long acting insulin analogues, glargine and detemir, in comparison with human insulin, IGF-1, and the super-mitogenic insulin
Liheng Yang et al.
The Journal of biological chemistry, 291(8), 3905-3917 (2015-12-20)
The normal cellular prion protein (PrP) is a glycosylphosphatidylinositol (GPI)-anchored cell surface glycoprotein. However, in pancreatic ductal adenocarcinoma cell lines, such as BxPC-3, PrP exists as a pro-PrP retaining its glycosylphosphatidylinositol (GPI) peptide signaling sequence. Here, we report the identification
D L Christie et al.
The Biochemical journal, 270(1), 57-61 (1990-08-15)
Chromaffin-granule membranes were separated into insoluble and soluble fractions after extraction with lithium di-iodosalicylate (LDIS). These fractions were characterized by one- and two-dimensional gel electrophoresis, and glycoproteins were detected after electroblotting with peroxidase-labelled concanavalin A and wheat-germ agglutinin (WGA). The
María-Ángeles Cortés-Gómez et al.
International journal of molecular sciences, 24(2) (2023-01-22)
In Alzheimer's disease (AD), the reduction in acetylcholinesterase (AChE) enzymatic activity is not paralleled with changes in its protein levels, suggesting the presence of a considerable enzymatically inactive pool in the brain. In the present study, we validated previous findings
Cynthia Tang et al.
Communications biology, 4(1), 161-161 (2021-02-07)
Mutations in CLN3 lead to photoreceptor cell loss in CLN3 disease, a lysosomal storage disorder characterized by childhood-onset vision loss, neurological impairment, and premature death. However, how CLN3 mutations cause photoreceptor cell death is not known. Here, we show that

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