生物来源
rabbit
质量水平
抗体形式
affinity purified immunoglobulin
抗体产品类型
primary antibodies
克隆
polyclonal
纯化方式
affinity chromatography
种属反应性
rat, human
制造商/商品名称
Chemicon®
技术
western blot: suitable
NCBI登记号
UniProt登记号
运输
dry ice
靶向翻译后修饰
unmodified
基因信息
human ... PLXNA1(5361)
特异性
Plexin-A1. The immunogen sequence has low homology with other plexin family members.
免疫原
Synthetic peptide from the semaphorin domain of human plexin-A1.
应用
Research Category
Neuroscience
Neuroscience
Research Sub Category
Growth Cones & Axon Guidance
Growth Cones & Axon Guidance
This Anti-Plexin-A1 Antibody is validated for use in WB for the detection of Plexin-A1.
Western blot: 1:1,000 on neonatal rat brain and COS-7 cells transfected with mouse Plexin-A1. The antibody reacts with the ~220 kDa protein. The suggested antibody diluent is PBS containing 5% non-fat milk and 0.04% Tween 20. Other bands may be present depending on the concentration of antibody and sample used.
Optimal working dilutions must be determined by the end user.
Optimal working dilutions must be determined by the end user.
外形
Affinity purified immunoglobulin. Liquid in PBS containing 50% glycerol, 1 mg/mL BSA and 0.05% sodium azide.
储存及稳定性
Maintain at -20°C in undiluted aliquots for up to 6 months after date of receipt. Avoid repeated freeze/thaw cycles.
法律信息
CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany
免责声明
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.
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储存分类代码
10 - Combustible liquids
WGK
WGK 2
Human molecular genetics, 26(11), 2006-2017 (2017-03-24)
The olfacto-genital syndrome (Kallmann syndrome) associates congenital hypogonadism due to gonadotropin-releasing hormone (GnRH) deficiency and anosmia. This is a genetically heterogeneous developmental disease with various modes of transmission, including oligogenic inheritance. Previous reports have involved defective cell signaling by semaphorin-3A
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