ABN1723
Anti-RTN3 (R458)
from rabbit
Synonym(s):
Reticulon-3, HAP, Homolog of ASY protein, Neuroendocrine-specific protein-like 2, Neuroendocrine-specific protein-like II, NSP-like protein 2, NSP-like protein II, NSPLII
Sign Into View Organizational & Contract Pricing
All Photos(3)
About This Item
UNSPSC Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41
Recommended Products
biological source
rabbit
Quality Level
antibody form
unpurified
antibody product type
primary antibodies
clone
polyclonal
species reactivity
mouse, human
species reactivity (predicted by homology)
rat (based on 100% sequence homology), chimpanzee (based on 100% sequence homology)
technique(s)
immunofluorescence: suitable
immunohistochemistry: suitable
immunoprecipitation (IP): suitable
western blot: suitable
NCBI accession no.
UniProt accession no.
shipped in
dry ice
target post-translational modification
unmodified
Gene Information
human ... RTN3(10313)
General description
Reticulon-3 (UniProt O95197; also known as HAP, Homolog of ASY protein, Neuroendocrine-specific protein-like 2, Neuroendocrine-specific protein-like II, NSP-like protein 2, NSP-like protein II, NSPLII) is encoded by the RTN3 (also known as ASYIP, NSPL2) gene (Gene ID 10313) in human. Reticulon-3/RTN3 belongs to the RTN family of proteins characterized by their C-terminal reticulon homolog domain (RHD; a.a. 844-1032 in RTN3). There exist four mammalian reticulons (RTN1-4), with each member having multiple spliced isoforms. RTN3 is expressed in neurons and localized in axons and growth cones. RTN3 overexpression in neurons results in reduced amyloid deposition in murine models of Alzheimer′s disease (AD). Consistently, RTN3 deficiency elevates BACE1 protein level and enhances amyloid deposition in AD mice that express human mutant APP and presenilin-1 transgenes. Human RTN3 is a multipass ER and golgi membrane protein with 3 membrane helical regions (a.a. 864-997, 948-968, 973-993) and four cytoplasmic regions (a.a. 2-863, 888-947, 969-972, 994-1032). Its C-terminal RHD mediates interaction with FADD (a.a. 987-1032) and BACE1 (a.a.1000-1002). Alternative splicings generate 7 isoforms (UniProt O95197-1 througth O95197-7).
Specificity
Target specificity of this rabbit polyclonal antiserum has been verified by Western blotting analysis of RNAi-mediated RTN3-knockdown in Swedish mutant APP-expressing 125.3 cells and tissue samples from RTN3-knockout mice. Immunogen sequence is located near the C-terminus of all human/mouse/rat isoforms reported by UniProt (O95197, O95197, Q9ES97) with the exception of human isoforms 5 and 6 (O95197-5 and O95197-6), which lack the target sequence.
Immunogen
Conjugated linear peptide corresponding to a sequence near the C-terminus of human RTN3.
Application
Anti-RTN3 (R458) Antibody, Cat. No. ABN1723, is a highly specific rabbit polyclonal antibody that targets RTN3 and has been tested in and Immunofluorescence, Immunohistochemistry, Immunoprecipitation, and Western Blotting.
Immunofluorescence Analysis: A 1:2,000 dilution from a representative lot immunostained dystrophic neurites in Alzheimer′s diseased (AD) human frozen brain tissue sections by fluorescent immunohistochemistry (Courtesy of Wanxia He, The Cleveland Clinic Foundation, U.S.A.).
Immunohistochemistry Analysis: A 1:2,000 dilution from a representative lot immunostained dystrophic neurites in Alzheimer′s diseased (AD) human frozen brain tissue sections (Courtesy of Wanxia He, The Cleveland Clinic Foundation, U.S.A.).
Western Blotting Analysis: A 1:2,000 dilution from a representative lot detected RTN3 isoforms in 50 µg of brain tissue lysate from a wild-type, but not RTN3-knockout, mouse (Courtesy of Wanxia He, The Cleveland Clinic Foundation, U.S.A.).
Immunofluorescence Analysis: A representative lot detected RTN3 immunoreactivity partially co-localized with that of BACE1 in mouse brain tissue sections (He, W., et al. (2004). Nat. Med.10(9):959-965).
Immunohistochemistry Analysis: A representative lot detected RTN3 immunoreactivity enriched in grey matter neuronal cell bodies of human brain tissue sections (He, W., et al. (2004). Nat. Med.10(9):959-965).
Immunoprecipitation Analysis: A representative lot co-immunoprecipitated BACE1 with RTN3 from HEK293 and human frontal cortex membrane extracts (He, W., et al. (2004). Nat. Med.10(9):959-965).
Western Blotting Analysis: A representative lot detected RTN3 isoforms expression in multiple mouse tissues, including broadly expressed ~25 kDa RTN3-A1 (UniProt Q9ES97-3), ~100 kDa fat tissue-specific RTN3-AL (UniProt Q9ES97-1), ~95 kDa brain-specific RTN3-B, and ~27 kDa RTN3-A2 (UniProt Q9ES97-4) in spinal cord. RTN3 target bands were not detected in tissue samples from RTN3-knockout mice (Shi, Q., et al. (2014). J. Neurosci. 34(42):13954-13962; He, W., et al. (2004). Nat. Med.10(9):959-965).
Western Blotting Analysis: A representative lot detected RTN3 isoform 3 (UniProt O95197-3) wild-type and mutant constructs expression. Membrane integration was affected by L71K/L72K mutation or deletion of N-terminal 97 a.a., while truncation of the first 61 a.a. did not affect embrane integration. Western blotting analysis of protease K-digested HEK293 microsomal preparation indicated a cytoplasmic orientation of the C-terminal end (He, W., et al. (2007). J. Biol. Chem. 282(40):29144-29151).
Western Blotting Analysis: A representative lot detected RTN3 in BACE1 immunoprecipitate from HEK293 membrane extract. A bimodal distribution showing RTN3 enrichment in subcellular fractions containing Golgi proteins and those containing ER markers was seen (He, W., et al. (2004). Nat. Med.10(9):959-965).
Western Blotting Analysis: A representative lot detected RNAi-mediated RTN3-knockdown in Swedish mutant APP-expressing 125.3 cells (He, W., et al. (2004). Nat. Med.10(9):959-965).
Immunohistochemistry Analysis: A 1:2,000 dilution from a representative lot immunostained dystrophic neurites in Alzheimer′s diseased (AD) human frozen brain tissue sections (Courtesy of Wanxia He, The Cleveland Clinic Foundation, U.S.A.).
Western Blotting Analysis: A 1:2,000 dilution from a representative lot detected RTN3 isoforms in 50 µg of brain tissue lysate from a wild-type, but not RTN3-knockout, mouse (Courtesy of Wanxia He, The Cleveland Clinic Foundation, U.S.A.).
Immunofluorescence Analysis: A representative lot detected RTN3 immunoreactivity partially co-localized with that of BACE1 in mouse brain tissue sections (He, W., et al. (2004). Nat. Med.10(9):959-965).
Immunohistochemistry Analysis: A representative lot detected RTN3 immunoreactivity enriched in grey matter neuronal cell bodies of human brain tissue sections (He, W., et al. (2004). Nat. Med.10(9):959-965).
Immunoprecipitation Analysis: A representative lot co-immunoprecipitated BACE1 with RTN3 from HEK293 and human frontal cortex membrane extracts (He, W., et al. (2004). Nat. Med.10(9):959-965).
Western Blotting Analysis: A representative lot detected RTN3 isoforms expression in multiple mouse tissues, including broadly expressed ~25 kDa RTN3-A1 (UniProt Q9ES97-3), ~100 kDa fat tissue-specific RTN3-AL (UniProt Q9ES97-1), ~95 kDa brain-specific RTN3-B, and ~27 kDa RTN3-A2 (UniProt Q9ES97-4) in spinal cord. RTN3 target bands were not detected in tissue samples from RTN3-knockout mice (Shi, Q., et al. (2014). J. Neurosci. 34(42):13954-13962; He, W., et al. (2004). Nat. Med.10(9):959-965).
Western Blotting Analysis: A representative lot detected RTN3 isoform 3 (UniProt O95197-3) wild-type and mutant constructs expression. Membrane integration was affected by L71K/L72K mutation or deletion of N-terminal 97 a.a., while truncation of the first 61 a.a. did not affect embrane integration. Western blotting analysis of protease K-digested HEK293 microsomal preparation indicated a cytoplasmic orientation of the C-terminal end (He, W., et al. (2007). J. Biol. Chem. 282(40):29144-29151).
Western Blotting Analysis: A representative lot detected RTN3 in BACE1 immunoprecipitate from HEK293 membrane extract. A bimodal distribution showing RTN3 enrichment in subcellular fractions containing Golgi proteins and those containing ER markers was seen (He, W., et al. (2004). Nat. Med.10(9):959-965).
Western Blotting Analysis: A representative lot detected RNAi-mediated RTN3-knockdown in Swedish mutant APP-expressing 125.3 cells (He, W., et al. (2004). Nat. Med.10(9):959-965).
Research Category
Neuroscience
Neuroscience
Quality
Evaluated by Western Blotting in mouse brain tissue lysates.
Western Blotting Analysis: A 1:500 dilution of this antibody detected RTN3 isoforms in 50 µg of brain tissue lysate from a wild-type, but not RTN3-knockout, mouse.
Western Blotting Analysis: A 1:500 dilution of this antibody detected RTN3 isoforms in 50 µg of brain tissue lysate from a wild-type, but not RTN3-knockout, mouse.
Target description
~95/25 kDa observed. 112.5/110.5/25.48/27.44/100.7 kDa (human isoform 1/2/3/4/7), 103.7/101.8/25.30/27.26/68.64 kDa (mouse isoform 1/2/3/4/5), 101.4/25.30 kDa (rat isoform 1/2) calculated. Uncharacterized bands may be observed in some lysate(s).
Physical form
Format: Unpurified
Rabbit polyclonal antibody serum with 0.05% sodium azide.
Unpurified.
Storage and Stability
Stable for 1 year at -20°C from date of receipt.
Handling Recommendations: Upon receipt and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.
Handling Recommendations: Upon receipt and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.
Other Notes
Concentration: Please refer to lot specific datasheet.
Disclaimer
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.
Not finding the right product?
Try our Product Selector Tool.
Storage Class Code
12 - Non Combustible Liquids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Youtong Huang et al.
STAR protocols, 3(4), 101891-101891 (2022-12-07)
Here, we describe a highly adaptable toolbox for characterizing and analyzing molecular and histopathological changes in Alzheimer's disease (AD) mouse models. We detail optimized and streamlined approaches from sample preparation to image analysis to facilitate reproducible analyses. We also describe
Youtong Huang et al.
Nature immunology, 22(5), 586-594 (2021-04-17)
Two microglial TAM receptor tyrosine kinases, Axl and Mer, have been linked to Alzheimer's disease, but their roles in disease have not been tested experimentally. We find that in Alzheimer's disease and its mouse models, induced expression of Axl and
Panpan Wang et al.
Molecular neurodegeneration, 19(1), 62-62 (2024-08-26)
Although WD repeat domain 45 (WDR45) mutations have been linked to β -propeller protein-associated neurodegeneration (BPAN), the precise molecular and cellular mechanisms behind this disease remain elusive. This study aims to shed light on the impacts of WDR45-deficiency on neurodegeneration
Tarique R Bagalkot et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 41(2), 234-250 (2020-11-26)
Dopamine transporter (DAT) controls dopamine neurotransmission by clearing synaptically released dopamine. However, trafficking itineraries of DAT, which determine its cell-surface concentration near synapses, are poorly characterized. It is especially unknown how DAT is transported between spatially distant midbrain somatodendritic and
Sharif Alhajlah et al.
Cells, 10(8) (2021-08-28)
CNS neurons are generally incapable of regenerating their axons after injury due to several intrinsic and extrinsic factors, including the presence of axon growth inhibitory molecules. One such potent inhibitor of CNS axon regeneration is Reticulon (RTN) 4 or Nogo-A.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service