ABN363
Anti-Myelin Protein P0 Antibody
from rabbit, purified by affinity chromatography
Synonim(y):
Myelin protein P0, Myelin peripheral protein, MPP, Myelin protein zero
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About This Item
Kod UNSPSC:
12352203
eCl@ss:
32160702
NACRES:
NA.41
klon:
polyclonal
application:
IHC
WB
WB
reaktywność gatunkowa:
rat, mouse
metody:
immunohistochemistry: suitable (paraffin)
western blot: suitable
western blot: suitable
citations:
6
Polecane produkty
pochodzenie biologiczne
rabbit
Poziom jakości
forma przeciwciała
affinity isolated antibody
rodzaj przeciwciała
primary antibodies
klon
polyclonal
oczyszczone przez
affinity chromatography
reaktywność gatunkowa
rat, mouse
reaktywność gatunkowa (przewidywana na podstawie homologii)
bovine (based on 100% sequence homology), horse (based on 100% sequence homology), human (based on 100% sequence homology)
metody
immunohistochemistry: suitable (paraffin)
western blot: suitable
numer dostępu NCBI
numer dostępu UniProt
Warunki transportu
wet ice
docelowa modyfikacja potranslacyjna
unmodified
informacje o genach
human ... MPZ(4359)
Opis ogólny
Myelin protein P0 is also called Myelin peripheral protein (MPP) and Myelin protein zero (MPZ). Myelin protein P0 is found only in peripheral nervous system and is involved in the creation of an extracellular membrane face which guides the wrapping process that eventually leads to the compaction of adjacent lamellae. Myelin protein P0 is related to several disease states including Charcot-Marie-Tooth disease 1B (CMT1B), Charcot-Marie-Tooth disease 2I (CMT2I), Charcot-Marie-Tooth disease 2J (CMT2J), Adie pupil (ADIEP), Charcot-Marie-Tooth disease, dominant, intermediate type, D (CMTDID), Dejerine-Sottas syndrome (DSS), Congenital hypomyelination neuropathy (CHN), and Roussy-Levy syndrome (ROULS).
Immunogen
KLH-conjugated linear peptide corresponding to the extracellular domain of human Myelin protein P0.
Zastosowanie
Anti-Myelin Protein P0 Antibody is a highly specific rabbit polyclonal antibody, that targets Myelin Protein & has been tested in western blotting & IHC (Paraffin).
Immunohistochemistry Analysis: A 1:2,000 dilution of this antibody detected Myelin protein P0 in rat spinal cord sections.
Research Category
Neuroscience
Neuroscience
Research Sub Category
Developmental Neuroscience
Developmental Neuroscience
Jakość
Evaluated by Western Blotting in rat spinal cord tissue lysate.
Western Blotting Analysis: A 1:5,000 dilution of this antibody detected Myelin protein P0 in 10 µg of rat spinal cord tissue lysate.
Western Blotting Analysis: A 1:5,000 dilution of this antibody detected Myelin protein P0 in 10 µg of rat spinal cord tissue lysate.
Opis wartości docelowych
~30 kDa observed
Postać fizyczna
Affinity purified
Purified rabbit polyclonal in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.
Przechowywanie i stabilność
Stable for 1 year at 2-8°C from date of receipt.
Oświadczenie o zrzeczeniu się odpowiedzialności
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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Kod klasy składowania
12 - Non Combustible Liquids
Klasa zagrożenia wodnego (WGK)
WGK 1
Temperatura zapłonu (°F)
Not applicable
Temperatura zapłonu (°C)
Not applicable
Certyfikaty analizy (CoA)
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Masz już ten produkt?
Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.
Ying Zou et al.
Cell & bioscience, 11(1), 210-210 (2021-12-16)
Silent information regulator 6 (SIRT6) is a mammalian homolog of the nicotinamide adenine dinucleotide (NAD)-dependent deacetylase sirtuin family. Prior evidences suggested that the anti-inflammatory function of SIRT6 after spinal cord and brain injury, and it plays a crucial role in
Sandra Murphy et al.
Journal of proteomics, 191, 212-227 (2018-02-07)
The highly progressive neuromuscular disorder dystrophinopathy is triggered by primary abnormalities in the Dmd gene, which causes cytoskeletal instability and loss of sarcolemmal integrity. Comparative organellar proteomics was employed to identify sarcolemma-associated proteins with an altered concentration in dystrophic muscle
Jiawei Xu et al.
Journal of neuroinflammation, 18(1), 234-234 (2021-10-17)
Plenty of macrophages are recruited to the injured nerve to play key roles in the immunoreaction and engulf the debris of degenerated axons and myelin during Wallerian degeneration, thus creating a conducive microenvironment for nerve regeneration. Recently, drugs targeting the
Erin-Mai F Lim et al.
Proceedings of the National Academy of Sciences of the United States of America, 114(9), E1707-E1716 (2017-02-01)
AlphaB-crystallin (αBC) is a small heat shock protein that is constitutively expressed by peripheral nervous system (PNS) axons and Schwann cells. To determine what role this crystallin plays after peripheral nerve damage, we found that loss of αBC impaired remyelination
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