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AC-0368A

p62 (Sequestosome-1) (EP396) Rabbit Monoclonal Primary Antibody

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Über diesen Artikel

NACRES:
NA.41
UNSPSC Code:
12352203
Clone:
monoclonal
Technique(s):
immunohistochemistry (formalin-fixed, paraffin-embedded sections): 1:100-1:200
Application:
IHC (p)
Citations:
-
Preise und Verfügbarkeit sind derzeit nicht verfügbar.
Technischer Dienst
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biological source

rabbit

Quality Segment

antibody form

Ig fraction of antiserum

clone

monoclonal

description

For In Vitro Diagnostic Use in Select Regions (See Chart)

form

buffered aqueous solution

technique(s)

immunohistochemistry (formalin-fixed, paraffin-embedded sections): 1:100-1:200

shipped in

wet ice

storage temp.

2-8°C

visualization

(nuclear,cytoplasm)

General description

P62, also known as Sequestosome-1, is a ubiquitin-binding adapter protein involved in the delivery of ubiquitin-bound protein and organelles to the autophagosome for lysosomal degradation during autophagy. Mutations in p62 have been linked to Paget′s disease and neurodegenerative disorders. P62 is typically degraded during the autophagy process, but can accumulate and/or overexpressed in autophagy-deficient cells. Presence of p62 cytosolic aggregate is used as a marker for autophagy deficiency. Defective autophagy increase oxidative stress and may play a role in tumorigenesis. P62 immunohistochemistry (IHC) diagnostic utility was established for identifying hepatocellular carcinoma (HCC). P62 demonstrates superior sensitivity for HCC compared against glypican-3. Positive p62 staining was found in 100% of HCC but were negative in all non-tumor areas and cirrhotic nodules. Furthermore, a panel consisting of p62, aminoacylase 1, and glypican-3 provides high sensitivity (93.8%) and specificity (95.2%) in the differential diagnosis between well differentiated HCC and high grade dysplastic nodules. P62 expression can also aid in diagnosing drug-induced autophagic vacuolar myopathies. An optimal threshold of at least 11.5% positive fibers provided 100% sensitivity and 100% specificity for autophagic myopathy. While current diagnostic criteria require identification of autophagic vacuoles by electron microscopy, diagnosis with p62 IHC could expedite the process and reduce costliness and large sampling variance associated with electron microscopy.

Physical form

Solution in Tris Buffer, pH 7.3-7.7, with 1% BSA and &lt0.1% Sodium Azide

Analysis Note


IVD

IVD

IVD

RUO

Other Notes

For a copy of the IFU and CofA contact IVDorder@ABCAM.com

For Technical Service please contact: 800-665-7284 or email: service@cellmarque.com

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Dieser Artikel
AC-0368AB2991MABC32
biological source

rabbit

biological source

rabbit

biological source

rabbit

biological source

mouse

clone

monoclonal

clone

monoclonal

clone

polyclonal

clone

11C9.2, monoclonal

antibody form

Ig fraction of antiserum

antibody form

Ig fraction of antiserum

antibody form

affinity isolated antibody

antibody form

purified antibody

shipped in

wet ice

shipped in

wet ice

shipped in

wet ice

shipped in

wet ice

form

buffered aqueous solution

form

buffered aqueous solution

form

-

form

-

technique(s)

immunohistochemistry (formalin-fixed, paraffin-embedded sections): 1:100-1:200

technique(s)

immunohistochemistry (formalin-fixed, paraffin-embedded sections): suitable

technique(s)

immunocytochemistry: suitable, western blot: suitable

technique(s)

flow cytometry: suitable, immunocytochemistry: suitable, western blot: suitable


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Lagerklasse

10 - Combustible liquids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable



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