Saltar al contenido
Merck

MAB329-C

Anti-Synaptophysin Antibody, clone SP15 (Ascites Free)

clone SP15, from mouse

Sinónimos:

Major synaptic vesicle protein p38, Synaptophysin

Iniciar sesión para ver los precios por organización y contrato.

Seleccione un Tamaño


Acerca de este artículo

UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Conjugate:
unconjugated
Clone:
SP15, monoclonal
Application:
ELISA, ICC, IHC, WB
Citations:
9
Servicio técnico
¿Necesita ayuda? Nuestro equipo de científicos experimentados está aquí para ayudarle.
Permítanos ayudarle
Servicio técnico
¿Necesita ayuda? Nuestro equipo de científicos experimentados está aquí para ayudarle.
Permítanos ayudarle

biological source

mouse

conjugate

unconjugated

antibody form

purified antibody

antibody product type

primary antibodies

clone

SP15, monoclonal

species reactivity

human, monkey, feline, rat, mouse

technique(s)

ELISA: suitable, immunocytochemistry: suitable, immunohistochemistry: suitable, western blot: suitable

isotype

IgMκ

NCBI accession no.

UniProt accession no.

target post-translational modification

unmodified

Quality Level

Gene Information

human ... SYP(6855)

General description

Synaptophysin (UniProt P08247; also known as Major synaptic vesicle protein p38) is encoded by the SYP (also known as MRX96, MRXSYP) gene (Gene ID 6855) in human. Synaptophysin is a 38 kDa four-transmembrane glycoprotein on synaptic vesicle (SV) with both its N- and C-termini exposed cytoplasmically. Synaptophysin forms homomultimers in the SV membrane and is heavily phosphorylated on tyrosine residues in its C-terminal pentapeptide repeats. Synaptophysin is also known to interact with SV v-SNARE protein synaptobrevin II (sybII) when sybII is not engaged with other SNARE proteins, suggesting a role of synaptophysin in sybII retrieval during SV endocytosis. Consistently, synaptophysin-knockout neurons display reduced levels of sybII at their nerve terminals.
~34 kDa observed

Immunogen

Human brain proteins immunoprecipitated with EP10 (Cat. No. MAB332).

Application

Research Category
Neuroscience
Research Sub Category
Developmental Neuroscience
This Anti-Synaptophysin Antibody, clone SP15 (Ascites Free) is validated for use in Western Blotting, Immunohistochemistry, Immunocytochemistry, ELISA for the detection of Synaptophysin.
Western Blotting Analysis: 1.0 µg/mL from a representative lot detected Synaptophysin in 10 µg of human brain tissue lysate.
Western Blotting Analysis: A representative lot detected synaptophysin in rat hippocampal tissue extracts (Lin, D., et al. (2012). Behav. Brain Res. 228(2):319-327).
Western Blotting Analysis: Representative lots detected synaptophysin in mouse brain synaptosomes preparations (Shim, S.Y., et al. (2008). J. Neurosci. 28(14):3604-3614).
Western Blotting Analysis: A representative lot detected synaptophysin in the large dense-core vesicles-containing fractions obtained by sucrose gradient centrifugation of rat brain median eminence (ME) neuroterminals preparations (Yin, W., et al. (2007). Exp. Biol. Med. (Maywood). 232(5):662-673).
Immunohistochemistry Analysis: A representative lot detected a stronger synaptophysin immunoreactivity in the inner molecular layer of frozen dentate gyrus sections from a 3-week old monkey, while a stronger immunoreactivity was seen in the outer molecular layer of dentate gyrus sections from a 13-year old monkey (Lavenex, P., et al. (2007). Dev. Neurosci. 29(1-2):179–192).
Immunohistochemistry Analysis: A representative lot immunostained nerve terminals at palisade ending using cat extraocular muscle (EOM) whole mount sections (Konakci, K.Z., et al. (2005). Invest. Ophthalmol. Vis. Sci. 46(1):155-165).
Immunohistochemistry Analysis: A representative lot detected synaptophysin immunoreactivity in human brain tissue sections (Honer, W.G., et al. (1993). Brain Res. 609(1-2):9-20).
Immunocytochemistry Analysis: A representative lot detected punctate synatophysin immunoreactivity among cultured primary cerebrocortical neurons from rat embryos (Bragina, L., et al. (2006). J. Neurochem. 99(1):134-141.).
ELISA Analysis: Representative lots were employed as the capture antibody for the detection of synaptophysin in human temporal cortex, frontal cortex, and cerebellar cortex extracts by sandwich ELISA (Klucken, J., et al. (2006). Acta Neuropathol. 111(2):101-108; Fukumoto, H., et al. (2002). Arch. Neurol. 59(9):1381-1389).

Physical form

Format: Purified
Purified mouse monoclonal IgMκ antibody in PBS with 0.05% sodium azide.

Preparation Note

Stable for 1 year at 2-8°C from date of receipt.

Analysis Note

Evaluated by Western Blotting in rat brain tissue lysate.

Western Blotting Analysis: 1.0 µg/mL of this antibody detected Synaptophysin in 10 µg of rat brain tissue lysate.

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.

¿No encuentra el producto adecuado?  

Pruebe nuestro Herramienta de selección de productos.

Clase de almacenamiento

12 - Non Combustible Liquids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

¿Ya tiene este producto?

Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.

Visite la Librería de documentos

Novel localization of NMDA receptors within neuroendocrine gonadotropin-releasing hormone terminals.
Yin, W; Mendenhall, JM; Bratton, SB; Oung, T; Janssen, WG; Morrison, JH; Gore, AC
Experimental Biology and Medicine (Maywood, N.J.) null
Beta-secretase protein and activity are increased in the neocortex in Alzheimer disease.
Fukumoto, H; Cheung, BS; Hyman, BT; Irizarry, MC
Archives of Neurology null
Clinical and biochemical correlates of insoluble alpha-synuclein in dementia with Lewy bodies.
Klucken, J; Ingelsson, M; Shin, Y; Irizarry, MC; Hedley-Whyte, ET; Frosch, M; Growdon et al.
Acta neuropathologica null
Postnatal development of the primate hippocampal formation.
Lavenex, P; Banta Lavenex, P; Amaral, DG
Developmental Neuroscience null
Molecular characteristics suggest an effector function of palisade endings in extraocular muscles.
Konakci, KZ; Streicher, J; Hoetzenecker, W; Blumer, MJ; Lukas, JR; Blumer, R
Investigative Ophthalmology & Visual Science null

Contenido relacionado

Alzheimer’s Disease is a progressively deteriorating disease. It manifests itself with memory loss, confusion, problems with judgment, planning, concentration, and personality changes; and in it’s later stages, a decline in physical abilities. The disease’s causes, cures, and preventions are unknown; however, key proteins likely involved in the degenerative mechanism have been identified. Alzheimer’s Disease is characterized by neuronal loss, alterations in neurotransmitter systems, and the presence of neurofibrillary tangles composed of abnormally hyperphosphorylated tau proteins. A prominent feature of Alzheimer’s Disease is the formation of senile plaques in selected regions of the brain. The center of these plaques are composed mainly of fibrillary aggregates of a common, but not well understood, b amyloid peptides (Aβ). The Aβ peptides are generated from the larger amyloid-β precursor protein (APP) by the sequential action of β- and γ-secretase, and it is generally accepted that oligomeric forms of this Aβ are neurotoxic, resulting in disease progression.

"Mods – modifications – small alterations can have a big impact on form and function. In the motorsports world, stock vehicles are modified to enhance their performance. Modifications, or mods, to the engine, drive train, intake and exhaust components add up to provide phenomenal performance gains that can be measured as horsepower and torque increases, which yield a competitive advantage, and result in reduced run times. In biology, proteins undergo modifications that alter their function. Some proteins require the modifications in order to perform their function effectively, whether it’s a pro-protein that is cleaved to produce an active enzyme, or a protein that is phosphorylated to facilitate a signaling process. Other proteins, such as histones, undergo modifications that regulate gene expression and alter cellular function. There are several post translational modifications such as acetylation, methylation, phosphorylation, and ubiquitination that impact protein function and activity. As a result, the analysis of proteins and their post-translational modifications are particularly important for the study of normal and disease-associated processes. New antibodies to detect phospho Histidines are now available from EMD Millipore."

Número de artículo de comercio global

SKUGTIN
MAB329-C04055977297973

Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.

Póngase en contacto con el Servicio técnico