ABN1385
Anti-RanBP2 Antibody
from rabbit, purified by affinity chromatography
别名:
E3 SUMO-protein ligase RanBP2, 358 kDa nucleoporin, Nuclear pore complex protein Nup358, Nucleoporin Nup358, Ran-binding protein 2, RanBP2, p270, ADANE, ANE1, IIAE3, Transformation-Related Protein 2, TRP1, TRP2
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About This Item
生物来源
rabbit
抗体形式
affinity isolated antibody
抗体产品类型
primary antibodies
克隆
polyclonal
纯化方式
affinity chromatography
种属反应性
human, mouse
技术
immunofluorescence: suitable
immunohistochemistry: suitable
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 ... RANBP2(5903)
一般描述
RAN-binding protein 2 (RanBP2), also known as Nucleoporin Nup358 (Nup358), is encoded by the RANBP2 gene. RanBP2/Nup358 regulates functions of multiple cellular proteins through direct interactions via distinct domains. RanBP2/Nup358 binding partners include Ran GTPase, importin-beta, exportin-1/CRM1, red opsin, subunits of the proteasome, cox11, the kinesin-1 isoforms KIF5B and KIF5C, and E2 enzyme UBC9, where it functions as an E3 SUMO-protein ligase and facilitates subsequent SUMOylation of protein substrates such as RanGAP and SP100.
免疫原
Epitope: Internal repeat IR1+2 domain (IR)
Recombinant protein corresponding to the internal repeat IR1+2 domain (IR) of human RanBP2.
应用
Anti-RanBP2 Antibody is an antibody against RanBP2 Antibody for use in Immunohistochemistry, Immunofluorescence.
Immunofluorescence Analysis: A 1:50 dilution from a representative lot detected RanBP2 in mouse retina cells (Paulo Ferreira, Duke University)
Immunofluorescence Analysis: A representative lot detected in mouse retina of RanBP2 transgenic mice (Cho, K., et al. (2014). JBC. 1-31).
Immunofluorescence Analysis: A representative lot detected in mouse retina of RanBP2 transgenic mice (Cho, K., et al. (2014). JBC. 1-31).
Research Category
Neuroscience
Neuroscience
Research Sub Category
Developmental Signaling
Developmental Signaling
质量
Evaluated by Immunohistochemistry in human retina tissue.
Immunohistochemistry Analysis: A 1:50 dilution of this antibody detected RanBP2 in human retina tissue.
Immunohistochemistry Analysis: A 1:50 dilution of this antibody detected RanBP2 in human retina tissue.
目标描述
358.2 kDa calculated
外形
Affinity purified
Purified rabbit polyclonal in buffer containing PBS with 0.05% sodium azide.
储存及稳定性
Stable for 1 year at 2-8°C from date of receipt.
其他说明
Concentration: Please refer to lot specific datasheet.
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
Cells, 10(9) (2021-09-29)
Cellular stress induces the formation of membraneless protein condensates in both the nucleus and cytoplasm. The nucleocytoplasmic transport of proteins mainly occurs through nuclear pore complexes (NPCs), whose efficiency is affected by various stress conditions. Here, we report that hyperosmotic
Journal of cell science, 134(6) (2021-02-05)
Ranbp2 (also known as Nup358) is a member of the nucleoporin family, which constitutes the nuclear pore complex. Ranbp2 localizes at the nuclear membrane and was recently reported at the axon initial segment (AIS). However, we show that the anti-Ranbp2
Human molecular genetics, 27(3), 407-420 (2017-12-01)
A critical challenge to deciphering the pathophysiology of neurodevelopmental disease is identifying which of the myriad abnormalities that emerge during CNS maturation persist to contribute to long-term brain dysfunction. Childhood-onset dystonia caused by a loss-of-function mutation in the AAA+ protein torsinA
The Journal of neuroscience : the official journal of the Society for Neuroscience, 41(9), 2024-2038 (2021-01-21)
DYT1 dystonia is a hereditary neurologic movement disorder characterized by uncontrollable muscle contractions. It is caused by a heterozygous mutation in Torsin A (TOR1A), a gene encoding a membrane-embedded ATPase. While animal models provide insights into disease mechanisms, significant species-dependent
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