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ITPR1 Mouse mAb

WGD-Z-2611584
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规格 价格
50ul ¥1286.00
100ul ¥2286.00
Overview
别名Inositol 1; 4; 5-trisphosphate-gated calcium channel ITPR1; IP3 receptor isoform 1; IP3R 1; InsP3R1; Inositol 1; 4; 5 trisphosphate receptor; Inositol 1; 4; 5-trisphosphate receptor type 1; Type 1 inositol 1; 4; 5-trisphosphate receptor; Type 1 InsP3 receptor
基因名IP3 Receptor
UniProt IDQ14643
反应种属Human,Mouse
应用WB,IHC-P
宿主Mouse
偶联物Unconjugated
修饰Unmodified
亚型IgG2a
克隆号7V3-J3-S5
克隆性Monoclonal Antibody
分子量Calculated MW: 313 kDa
纯化方式Affinity Purified
产品形式Liquid
推荐稀释比WB-1:1000; IHC-1:100-1:200
存储缓冲液Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.09% sodium azide
保存温度Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
背景信息Inositol 1,4,5-trisphosphate receptor type 1 (IP3 Receptor) is a large tetrameric intracellular calcium release channel primarily localized to the endoplasmic reticulum membrane. Each subunit contains a cytosolic N-terminal IP3-binding core and a C-terminal six-transmembrane channel domain that forms a calcium-selective pore. The receptor is activated by the binding of IP3, produced downstream of G-protein-coupled receptor signaling, which primes the channel for calcium-induced calcium release. This mechanism regulates critical cellular processes including synaptic plasticity, gene expression, and apoptosis. IP3 Receptor is highly expressed in cerebellar Purkinje cells and is essential for motor coordination. Pathogenic variants in the ITPR1 gene cause autosomal dominant spinocerebellar ataxias and Gillespie syndrome, characterized by cerebellar atrophy, ataxia, and developmental delay.
检测原理

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