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AB47085

Anti-Nogo A+B antibody

5

(10 Reviews)

|

(26 Publications)

Rabbit Polyclonal RTN4 antibody. Suitable for WB, IHC-P, ICC/IF and reacts with Human, Mouse, African green monkey, Rat samples. Cited in 26 publications. Immunogen corresponding to Synthetic Peptide within Human RTN4.

View Alternative Names

KIAA0886, NOGO, My043, SP1507, RTN4, Reticulon-4, Foocen, Neurite outgrowth inhibitor, Neuroendocrine-specific protein, Neuroendocrine-specific protein C homolog, RTN-x, Reticulon-5, Nogo protein, NSP

3 Images
Immunocytochemistry/ Immunofluorescence - Anti-Nogo A+B antibody (AB47085)
  • ICC/IF

Collaborator

Immunocytochemistry/ Immunofluorescence - Anti-Nogo A+B antibody (AB47085)

Immunocytochemistry stainning for Nogo A+B in Cor1 neural stem cells from mouse using Rabbit polyclonal to Nogo A+B (ab47085; 1/200 incubated for 2h at RT); Immunoreactivity was detected in cell-body as well as in neurites.

This image is courtesy of Carl Hobbs, King's College London, United Kingdom

Western blot - Anti-Nogo A+B antibody (AB47085)
  • WB

Unknown

Western blot - Anti-Nogo A+B antibody (AB47085)

All lanes:

Western blot - Anti-Nogo A+B antibody (ab47085) at 1/2000 dilution

Lane 1:

Human brain tissue lysate

Lane 2:

Mouse brain tissue lysate

Lane 3:

Rat brain tissue lysate

Observed band size: 41 kDa,43 kDa,48-50 kDa,>200 kDa

false

Immunocytochemistry/ Immunofluorescence - Anti-Nogo A+B antibody (AB47085)
  • ICC/IF

AbReview38987****

Immunocytochemistry/ Immunofluorescence - Anti-Nogo A+B antibody (AB47085)

ab47085 staining Nogo A+B in African Green Monkey COS-7 cells by ICC/IF (Immunocytochemistry/immunofluorescence). Cells were fixed with paraformaldehyde, permeabilized with 0.5% Triton X-100 and blocked with 3% BSA for 1 hour at 23°C. Samples were incubated with primary antibody (1/500 in PBS-BSA) for 1 hour at 23°C. An Alexa Fluor® 488-conjugated Goat anti-rabbit IgG polyclonal (1/1000) was used as the secondary antibody.

This image is courtesy of an anonymous Abreview

Key facts

Host species

Rabbit

Clonality

Polyclonal

Isotype

IgG

Carrier free

No

Reacts with

Mouse, Rat, Human, African green monkey

Applications

ICC/IF, WB, IHC-P

applications

Immunogen

Synthetic Peptide within Human RTN4. The exact immunogen used to generate this antibody is proprietary information.

Q9NQC3

Specificity

ab47085 recognises Nogo A and Nogo B2 and B1

Reactivity data

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Properties and storage information

Form
Liquid
Purification technique
Affinity purification Protein G
Storage buffer
Preservative: 0.02% Sodium azide Constituents: PBS
Shipped at conditions
Blue Ice
Appropriate short-term storage duration
1-2 weeks
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C
Aliquoting information
Upon delivery aliquot
Storage information
Avoid freeze / thaw cycle

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

Nogo A+B also known as Nogo Nogo B or Nogo-B refers to two isoforms of a protein that play a significant role in inhibiting axon regeneration and neurite outgrowth. Nogo A+B are part of the reticulon family of proteins where Nogo A has a molecular mass of approximately 220 kDa while Nogo B is around 55 kDa. These proteins are mainly expressed in the central nervous system specifically in the oligodendrocytes. Nogo A+B can be found on the surface of cells where they interact with specific receptors to carry out their functions.
Biological function summary

Nogo proteins influence cellular functions by acting as inhibitors of neuronal growth and regeneration. Nogo A and B interact with receptors like NgR1 to form a complex that suppresses the regrowth of damaged nerve fibers. It is suggested that this inhibition prevents unwanted and uncontrolled nerve growth maintaining the integrity of the neural architecture. The activity of these proteins is essential for maintaining the stability of cellular functions and structure particularly in neural tissues.

Pathways

These proteins are deeply ingrained in the signaling mechanisms that regulate the inhibition of axon regeneration. The Nogo signaling pathway is critical in modulating nerve growth where Nogo proteins interact with other proteins like RhoA and Rock which are essential in this pathway. This pathway plays an important role alongside the myelin-associated glycoprotein pathway both of which limit axon regeneration and guidance within the nervous system.

Nogo proteins have connections to conditions such as multiple sclerosis and spinal cord injury. In multiple sclerosis the expression of Nogo A limits neural repair contributing to the disease’s progression. Similarly in spinal cord injury increased levels of Nogo proteins inhibit the repair of neurons impeding recovery. These proteins are often studied alongside myelin-associated inhibitors such as MAG (Myelin-Associated Glycoprotein) which also plays a part in limiting neural regrowth further implicating Nogo proteins in these disorders.

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

Required to induce the formation and stabilization of endoplasmic reticulum (ER) tubules (PubMed : 24262037, PubMed : 25612671, PubMed : 27619977). They regulate membrane morphogenesis in the ER by promoting tubular ER production (PubMed : 24262037, PubMed : 25612671, PubMed : 27619977, PubMed : 27786289). They influence nuclear envelope expansion, nuclear pore complex formation and proper localization of inner nuclear membrane proteins (PubMed : 26906412). However each isoform have specific functions mainly depending on their tissue expression specificities (Probable).. Isoform A. Developmental neurite growth regulatory factor with a role as a negative regulator of axon-axon adhesion and growth, and as a facilitator of neurite branching. Regulates neurite fasciculation, branching and extension in the developing nervous system. Involved in down-regulation of growth, stabilization of wiring and restriction of plasticity in the adult CNS (PubMed : 10667797, PubMed : 11201742). Regulates the radial migration of cortical neurons via an RTN4R-LINGO1 containing receptor complex (By similarity). Acts as a negative regulator of central nervous system angiogenesis. Inhibits spreading, migration and sprouting of primary brain microvascular endothelial cells (MVECs). Also induces the retraction of MVECs lamellipodia and filopodia in a ROCK pathway-dependent manner (By similarity).. Isoform B. Mainly function in endothelial cells and vascular smooth muscle cells, is also involved in immune system regulation (Probable). Modulator of vascular remodeling, promotes the migration of endothelial cells but inhibits the migration of vascular smooth muscle cells. Regulates endothelial sphingolipid biosynthesis with direct effects on vascular function and blood pressure. Inhibits serine palmitoyltransferase, SPTLC1, the rate-limiting enzyme of the novo sphingolipid biosynthetic pathway, thereby controlling production of endothelial sphingosine-1-phosphate (S1P). Required to promote macrophage homing and functions such as cytokine/chemokine gene expression involved in angiogenesis, arteriogenesis and tissue repair. Mediates ICAM1 induced transendothelial migration of leukocytes such as monocytes and neutrophils and acute inflammation. Necessary for immune responses triggered by nucleic acid sensing TLRs, such as TLR9, is required for proper TLR9 location to endolysosomes. Also involved in immune response to LPS. Plays a role in liver regeneration through the modulation of hepatocytes proliferation (By similarity). Reduces the anti-apoptotic activity of Bcl-xl and Bcl-2. This is likely consecutive to their change in subcellular location, from the mitochondria to the endoplasmic reticulum, after binding and sequestration (PubMed : 11126360). With isoform C, inhibits BACE1 activity and amyloid precursor protein processing (PubMed : 16965550).. Isoform C. Regulates cardiomyocyte apoptosis upon hypoxic conditions (By similarity). With isoform B, inhibits BACE1 activity and amyloid precursor protein processing (PubMed : 16965550).
See full target information RTN4

Publications (26)

Recent publications for all applications. Explore the full list and refine your search

Cell reports 43:115053 PubMed39661521

2024

Legionella uses host Rab GTPases and BAP31 to create a unique ER niche.

Applications

Unspecified application

Species

Unspecified reactive species

Attinder Chadha,Yu Yanai,Hiromu Oide,Yuichi Wakana,Hiroki Inoue,Saradindu Saha,Manish Paul,Mitsuo Tagaya,Kohei Arasaki,Shaeri Mukherjee

Nature communications 15:9756 PubMed39528474

2024

Nonvesicular lipid transfer drives myelin growth in the central nervous system.

Applications

Unspecified application

Species

Unspecified reactive species

Jianping Wu,Georg Kislinger,Jerome Duschek,Ayşe Damla Durmaz,Benedikt Wefers,Ruoqing Feng,Karsten Nalbach,Wolfgang Wurst,Christian Behrends,Martina Schifferer,Mikael Simons

Redox biology 68:102944 PubMed37890359

2023

Nogo-B mediates endothelial oxidative stress and inflammation to promote coronary atherosclerosis in pressure-overloaded mouse hearts.

Applications

Unspecified application

Species

Unspecified reactive species

Yu Zhang,Jing-Jing Li,Rui Xu,Xin-Pei Wang,Xin-Yi Zhao,Yuan Fang,Yu-Peng Chen,Shan Ma,Xiao-Hui Di,Wei Wu,Gang She,Zheng-Da Pang,Yi-Dong Wang,Xing Zhang,Wenjun Xie,Xiu-Ling Deng,Xiao-Jun Du,Yi Zhang

The Journal of cell biology 222: PubMed37516910

2023

The nanoscale organization of reticulon 4 shapes local endoplasmic reticulum structure in situ.

Applications

Unspecified application

Species

Unspecified reactive species

Lukas A Fuentes,Zach Marin,Jonathan Tyson,David Baddeley,Joerg Bewersdorf

Nature 618:402-410 PubMed37225994

2023

Heteromeric clusters of ubiquitinated ER-shaping proteins drive ER-phagy.

Applications

Unspecified application

Species

Unspecified reactive species

Hector Foronda,Yangxue Fu,Adriana Covarrubias-Pinto,Hartmut T Bocker,Alexis González,Eric Seemann,Patricia Franzka,Andrea Bock,Ramachandra M Bhaskara,Lutz Liebmann,Marina E Hoffmann,Istvan Katona,Nicole Koch,Joachim Weis,Ingo Kurth,Joseph G Gleeson,Fulvio Reggiori,Gerhard Hummer,Michael M Kessels,Britta Qualmann,Muriel Mari,Ivan Dikić,Christian A Hübner

Biomedical optics express 13:6048-6060 PubMed36733753

2022

Super-multiplexing excitation spectral microscopy with multiple fluorescence bands.

Applications

Unspecified application

Species

Unspecified reactive species

Kun Chen,Wan Li,Ke Xu

The Journal of cell biology 221: PubMed34874453

2021

Reticulon-like REEP4 at the inner nuclear membrane promotes nuclear pore complex formation.

Applications

Unspecified application

Species

Unspecified reactive species

Banafsheh Golchoubian,Andreas Brunner,Helena Bragulat-Teixidor,Annett Neuner,Busra A Akarlar,Nurhan Ozlu,Anne-Lore Schlaitz

Neuron 110:452-469.e14 PubMed34798047

2021

Transcriptomic taxonomy and neurogenic trajectories of adult human, macaque, and pig hippocampal and entorhinal cells.

Applications

Unspecified application

Species

Unspecified reactive species

Daniel Franjic,Mario Skarica,Shaojie Ma,Jon I Arellano,Andrew T N Tebbenkamp,Jinmyung Choi,Chuan Xu,Qian Li,Yury M Morozov,David Andrijevic,Zvonimir Vrselja,Ana Spajic,Gabriel Santpere,Mingfeng Li,Shupei Zhang,Yang Liu,Joshua Spurrier,Le Zhang,Ivan Gudelj,Lucija Rapan,Hideyuki Takahashi,Anita Huttner,Rong Fan,Stephen M Strittmatter,Andre M M Sousa,Pasko Rakic,Nenad Sestan

International journal of molecular sciences 22: PubMed34638576

2021

Regulation of ER Composition and Extent, and Putative Action in Protein Networks by ER/NE Protein TMEM147.

Applications

Unspecified application

Species

Unspecified reactive species

Giannis Maimaris,Andri Christodoulou,Niovi Santama,Carsten Werner Lederer

eLife 10: PubMed34467852

2021

Endoplasmic reticulum tubules limit the size of misfolded protein condensates.

Applications

Unspecified application

Species

Unspecified reactive species

Smriti Parashar,Ravi Chidambaram,Shuliang Chen,Christina R Liem,Eric Griffis,Gerard G Lambert,Nathan C Shaner,Matthew Wortham,Jesse C Hay,Susan Ferro-Novick
View all publications

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