推荐产品
生物来源
rabbit
质量水平
抗体形式
serum
抗体产品类型
primary antibodies
克隆
polyclonal
形式
liquid
不包含
preservative
种属反应性（根据同源性预测）
all
制造商/商品名称
Calbiochem®
储存条件
OK to freeze
avoid repeated freeze/thaw cycles
同位素/亚型
IgG
运输
wet ice
储存温度
−20°C
靶向翻译后修饰
unmodified
一般描述
Anti-Ganglioside GM₂, rabbit polyclonal recognizes ganglioside GM₂ in a wide variety of species. It is validated for use in ELISA and TLC immunoblotting.
Rabbit polyclonal antibody supplied as undiluted serum. Recognizes the GM2 ganglioside.
Recognizes ganglioside GM2.
免疫原
purified, human ganglioside GM₂
应用
ELISA (1:200)
TLC Immunoblotting (1:100, colorimetric)
TLC Immunoblotting (1:100, colorimetric)
警告
Toxicity: Standard Handling (A)
其他说明
Does not cross-react with other carbohydrate epitopes. Variables associated with assay conditions will dictate the optimal working dilution.
Yoshino, H., et al. 1993. J. Neurochem. 61, 658.
Kusunoki, S., et al. 1987. Neurology 37, 1795.
Kusunoki, S., et al. 1987. Neurology 37, 1795.
法律信息
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
Yuehong Chen et al.
Journal of molecular medicine (Berlin, Germany), 96(12), 1359-1373 (2018-10-21)
Tay-Sachs disease (TSD) is a lethal lysosomal storage disease (LSD) caused by mutations in the HexA gene, which can lead to deficiency of β-hexosaminidase A (HexA) activity and consequent accumulation of its substrate, GM2 ganglioside. Recent reports that progranulin (PGRN)
Aleksandra Somogyi et al.
International journal of molecular sciences, 19(2) (2018-02-23)
Juvenile neuronal ceroid lipofuscinosis (JNCL) is caused by mutations in the CLN3 gene. Most JNCL patients exhibit a 1.02 kb genomic deletion removing exons 7 and 8 of this gene, which results in a truncated CLN3 protein carrying an aberrant
Meredith K Loth et al.
Neurobiology of disease, 85, 174-186 (2015-11-08)
Translocator protein (18 kDa), formerly known as the peripheral benzodiazepine receptor (PBR), has been extensively used as a biomarker of active brain disease and neuroinflammation. TSPO expression increases dramatically in glial cells, particularly in microglia and astrocytes, as a result
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