04-147
抗-ASC抗体,克隆2EI-7
clone 2EI-7, from mouse
别名:
Caspase recruitment domain-containing protein 5, PYD and CARD domain containing, PYD and CARD domain-containing protein, Target of methylation-induced silencing 1, apoptosis-associated speck-like protein containing a CARD, caspase recruitment domain prot
生物来源
mouse
质量水平
偶联物
unconjugated
抗体形式
purified antibody
抗体产品类型
primary antibodies
克隆
2EI-7, monoclonal
种属反应性
mouse
种属反应性(根据同源性预测)
human (based on 100% sequence homology)
技术
flow cytometry: suitable
western blot: suitable
同位素/亚型
IgG1κ
NCBI登记号
UniProt登记号
运输
wet ice
靶向翻译后修饰
unmodified
基因信息
human ... PYCARD(29108)
一般描述
~22 kDa
凋亡受包含分子和蛋白酶的胱天蛋白酶家族的死亡结构域(DD)和/或胱天蛋白酶募集结构域(CARD)调节。含有细胞死亡调节剂的CARD包括RAIDD,RICK,Bcl10,Apaf-1,ARC,半胱天冬酶-2和半胱天冬酶-9。已经在人和小鼠中鉴定出一种新的含有CARD结构域的蛋白质,并将其命名为ASC和TMS1。ASC/TMS1的不规则表达通过激活半胱天冬酶-9诱导细胞凋亡,并抑制人乳腺癌细胞的存活。ASC/TMS1的过表达诱导DNA片段化。ASC/TMS1在多种人类和小鼠组织中表达。
免疫原
全长重组人ASC。
表位:未知
应用
使用该抗ASC抗体,克隆2EI-7检测ASC,已验证可用于WB、FC。
研究子类别
凋亡-附加
凋亡-附加
研究类别
炎症 & 免疫学
炎症 & 免疫学
生化/生理作用
该抗体可识别ASC。
外形
形式:纯化
纯化的小鼠单克隆IgG1κ溶于含0.1 M Tris-甘氨酸(pH 7.4),150 mM NaCl和0.05%叠氮化钠的缓冲液中。
蛋白G纯化
制备说明
自收到之日起,在2-8°C条件下可稳定保存1年。
分析说明
对照
小鼠脾组织裂解液
小鼠脾组织裂解液
已通过蛋白质印迹在小鼠脾组织裂解液中进行了评估。
蛋白质印迹分析: 0.5 µg/mL的该抗体在小鼠脾组织裂解液中检测到ASC。
蛋白质印迹分析: 0.5 µg/mL的该抗体在小鼠脾组织裂解液中检测到ASC。
其他说明
浓度:请参考批次特异性浓缩物的分析证书。
免责声明
除非我们的产品目录或产品附带的其他公司文档另有说明,否则我们的产品仅供研究使用,不得用于任何其他目的,包括但不限于未经授权的商业用途、体外诊断用途、离体或体内治疗用途或任何类型的消费或应用于人类或动物。
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储存分类代码
12 - Non Combustible Liquids
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
Sung-Soo Jung et al.
American journal of physiology. Lung cellular and molecular physiology, 308(10), L1058-L1067 (2015-03-15)
Inflammasomes are cytosolic protein complexes that promote the cleavage of caspase-1, which leads to the maturation and secretion of proinflammatory cytokines, including interleukin-1β (IL-1β) and IL-18. Among the known inflammasomes, the nucleotide-binding domain, leucine-rich-containing family, pyrin domain-containing-3 (NLRP3)-dependent inflammasome is
Tiantian Tang et al.
Nature communications, 8(1), 202-202 (2017-08-06)
The NLRP3 inflammasome can sense different pathogens or danger signals, and has been reported to be involved in the development of many human diseases. Potassium efflux and mitochondrial damage are both reported to mediate NLRP3 inflammasome activation, but the underlying
Teneema Kuriakose et al.
Journal of immunology (Baltimore, Md. : 1950), 200(4), 1489-1495 (2018-01-13)
Innate immune sensing of influenza A virus (IAV) induces activation of various immune effector mechanisms, including the nucleotide and oligomerization domain, leucine-rich repeat-containing protein family, pyrin domain containing 3 (NLRP3) inflammasome and programmed cell death pathways. Although type I IFNs
Sonal Khare et al.
Nature immunology, 15(4), 343-353 (2014-02-18)
The innate immune system responds to infection and tissue damage by activating cytosolic sensory complexes called 'inflammasomes'. Cytosolic DNA is sensed by AIM2-like receptors (ALRs) during bacterial and viral infections and in autoimmune diseases. Subsequently, recruitment of the inflammasome adaptor
Wei Zhu et al.
Neuroscience, 343, 77-84 (2016-12-08)
Lipopolysaccharide (LPS) might affect the central nervous system by causing neuroinflammation, which subsequently leads to brain damage and dysfunction. In this study, we evaluated the role of nod-like receptor pyrin domain-containing protein 3 (NLRP3) inflammasome activation in long-term behavioral alterations
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