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P246

Monoclonal Anti-PSD95 antibody produced in mouse

clone 7E3-1B8, purified immunoglobulin, buffered aqueous solution

Synonym(e):

Anti-MRD62, Anti-PSD95, Anti-SAP-90, Anti-SAP90

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PackungsgrößeSKUVerfügbarkeitPreis
100 μL
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€ 706,00

Über diesen Artikel

UNSPSC Code:
12352203
NACRES:
NA.41
MDL number:
Conjugate:
unconjugated
Clone:
7E3-1B8, monoclonal
Application:
IF, IP, WB
Citations:
24

€ 706,00


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biological source

mouse

Quality Level

conjugate

unconjugated

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

7E3-1B8, monoclonal

form

buffered aqueous solution

mol wt

antigen 95 kDa

species reactivity

rat

technique(s)

immunofluorescence: 1:500, immunoprecipitation (IP): suitable, western blot: 1:2,000

isotype

IgG2a

UniProt accession no.

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Gene Information

rat ... Dlg4(29495)

General description

DLG4 (discs large MAGUK scaffold protein 4) gene codes for the postsynaptic density-95 (PSD95) protein. Postsynaptic density 95 (PSD-95), a synaptic scaffolding protein is also a membrane-associated guanylate kinase (MAGUK) family protein. It has three PDZ domains on the N terminus followed by a Src homology 3 (SH3) domain and a guanylate kinase (GK) domain. This gene is located on human chromosome 17p13.1.

Immunogen

recombinant rat PSD95 (post synaptic density 95 kDa).

Application

Applications in which this antibody has been used successfully, and the associated peer-reviewed papers, are given below.
Immunocytochemistry (1 paper)
Immunofluorescence (1 paper)
Western Blotting (1 paper)

Biochem/physiol Actions

Postsynaptic density 95 (PSD-95) plays a major role in bidirectional synaptic plasticity, an important process, essential for learning and memory. It exhibits increased dynamics upon induction of plasticity.
Reacts with both the recombinant and native rat PSD95. By immunofluorescence with rat hippocampal cells, a staining pattern coincident with NMDA receptor staining at synaptic sites consistent with its proposed role in receptor clustering is observed. Fixation with cold methanol is recommended.

Physical form

Solution in phosphate buffered saline containing 0.05% sodium azide.

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.

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Dieser Artikel
SAB5200003ABN998SAB1405717
biological source

mouse

biological source

mouse

biological source

rabbit

biological source

mouse

conjugate

unconjugated

conjugate

unconjugated

conjugate

-

conjugate

unconjugated

species reactivity

rat

species reactivity

mouse, rat, bovine

species reactivity

human

species reactivity

rat, human

clone

7E3-1B8, monoclonal

clone

7E3, monoclonal

clone

polyclonal

clone

polyclonal

antibody form

purified immunoglobulin

antibody form

purified immunoglobulin

antibody form

affinity isolated antibody

antibody form

purified immunoglobulin

Gene Information

rat ... Dlg4(29495)

Gene Information

rat ... Dlg4(29495)

Gene Information

human ... DLG4(1742)

Gene Information

human ... DLG4(1742)


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Lagerklasse

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)



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Verwandter Inhalt


Lindsey I Sinclair et al.
Neuropathology and applied neurobiology, 41(4), 533-543 (2015-01-07)
Cerebral ischaemia is the defining pathophysiological abnormality in most forms of vascular dementia (VAD), but the pathogenesis of the dementia remains poorly understood. In Alzheimer's disease (AD), there is early loss of synaptic proteins, but these have been little studied
Nora Overlack et al.
Vision research, 48(3), 400-412 (2007-10-10)
The human Usher syndrome (USH) is the most common form of combined deaf-blindness. Usher type I (USH1), the most severe form, is characterized by profound congenital deafness, constant vestibular dysfunction and prepubertal-onset of retinitis pigmentosa. Five corresponding genes of the
Lindsey I Sinclair et al.
Journal of Alzheimer's disease : JAD, 59(3), 1123-1137 (2017-07-22)
Possession of APOEɛ4 is a strong risk factor for late-onset Alzheimer's disease and is associated with loss of synaptic proteins in the elderly even in the absence of Alzheimer's disease. We hypothesized that ɛ4 allele possession in non-demented adults aged



Global Trade Item Number

SKUGTIN
P246-100UL04061834363590

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