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merck millipore,默克密理博,AB15012,Anti-Glycine Receptor α1 Antibody
产品名称:Anti-Glycine Receptor α1 Antibody
产品型号:AB15012
Anti-Glycine Receptor α1 Antibody detects level of Glycine Receptor α1 & has been published & validated for use in IH & WB.
merck millipore,默克密理博,AB15012,Anti-Glycine Receptor α1 Antibody
- 产品介绍
重要规格表
品种反应性 主要应用 宿主 格式 抗体类型 M, H WB, IHC Rb Purified Polyclonal Antibody 描述 产品目录编号 AB15012 品牌系列 Chemicon®
商名 - Chemicon
描述 Anti-Glycine Receptor α1 Antibody 产品信息 格式 Purified 演示 Liquid in PBS with 0.1% sodium azide. 应用 应用 Anti-Glycine Receptor α1 Antibody detects level of Glycine Receptor α1 & has been published & validated for use in IH & WB. 主要应用 - Western Blotting
- Immunohistochemistry
应用说明 Western blot: 0.5-1.0 ug/mL on extracts from Y79 cell lysate.
Immunohistochemistry on mouse spinal cord tissue sections.
Optimal working dilutions must be determined by the end user.生物信息 免疫原品种 Synthetic peptide. 宿主 Rabbit 特异性 Glycine Receptor alpha1. By Western blot the antibody recognizes a band at ~65 kDa in Y79 (human retinoblastoma) cell lysate. 品种反应性 MouseHuman 抗体类型 Polyclonal Antibody Entrez基因编号 - NM_000171.2
Entrez基因汇总 The inhibitory glycine receptor mediates postsynaptic inhibition in the spinal cord and other regions of the central nervous system. It is a pentameric receptor composed of alpha and beta subunits. The GLRB gene (MIM 138492) encodes the beta subunit of the receptor.[supplied by OMIM] 基因符号 - MGC138879
- GLRA1
- MGC138878
- STHE
纯化方法 Immunoaffinity purified UniProt编号 - P23415
UniProt汇总 FUNCTION: SwissProt: P23415 # The glycine receptor is a neurotransmitter-gated ion channel. Binding of glycine to its receptor increases the chloride conductance and thus produces hyperpolarization (inhibition of neuronal firing).
SIZE: 457 amino acids; 52624 Da
SUBUNIT: Pentamer composed of alpha and beta subunits.
SUBCELLULAR LOCATION: Cell junction, synapse, postsynaptic cell membrane; Multi-pass membrane protein.
DISEASE: SwissProt: P23415 # Defects in GLRA1 are a cause of startle disease (STHE) [MIM:149400]; also known as hereditary hyperekplexia or congenital stiff-person syndrome. STHE is a genetically heterogeneous neurologic disorder characterized by muscular rigidity of central nervous system origin, particularly in the neonatal period, and by an exaggerated startle response to unexpected acoustic or tactile stimuli. Inheritance can be autosomal dominant or recessive.
SIMILARITY: SwissProt: P23415 ## Belongs to the ligand-gated ionic channel (TC 1.A.9) family.
MISCELLANEOUS: The alpha subunit binds strychnine.产品使用声明 使用声明 - Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
储存和货运信息 存储条件 Maintain at 2-8°C in undiluted aliquots for up to 6 months after date of receipt 包装信息 数量 100 µg
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