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Key Documents

AB825

Sigma-Aldrich

Anti-Apolipoprotein J Antibody

Chemicon®, from goat

Synonyme(s) :

Clusterin, ApoJ

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About This Item

Code UNSPSC :
12352203
eCl@ss :
32160702
Nomenclature NACRES :
NA.41

Source biologique

goat

Niveau de qualité

100

Forme d'anticorps

affinity purified immunoglobulin

Type de produit anticorps

primary antibodies

Clone

polyclonal

Produit purifié par

affinity chromatography

Espèces réactives

human

Fabricant/nom de marque

Chemicon®

Technique(s)

ELISA: suitable
immunohistochemistry: suitable (paraffin)
immunoprecipitation (IP): suitable
western blot: suitable

Numéro d'accès NCBI

NM_001831.2
NM_203339.1

Numéro d'accès UniProt

P10909

Conditions d'expédition

wet ice

Modification post-traductionnelle de la cible

unmodified

Informations sur le gène

human ... CLU(1191)

Spécificité

Apolipoprotein J, Human. Negligible cross reactivity to Apo A-I, A-II, B, C-I, C-II, C-III, and E by ELISA. Negligible non-specific cross-reaction with other human serum proteins.

Immunogène

Apolipoprotein J, purified from human plasma.

Application

Anti-Apolipoprotein J Antibody is an antibody against Apolipoprotein J for use in ELISA, IP, WB, IH(P).
Immunoblotting: 1:5,000-1:10,000

Immunohistochemistry on paraffin embedded tissue: 1:50-1:200

Immunoprecipitation

ELISA: 1:5,000-1:10,000

Optimal working dilutions must be determined by end user.
Research Category
Metabolism
Research Sub Category
Lipid Metabolism & Weight Regulation

Forme physique

Affinity purified immunoglobulin. Liquid in 0.125 M Sodium Borate buffer, 0.075 M Sodium Chloride, 0.005 M EDTA, pH 8.0, with 0.01% sodium azide.

Stockage et stabilité

Maintain at 2-8°C in undiluted aliquots for several weeks. For extended storage mix with an equal volume of glycerol, aliquot contents and freeze at -20°C or below for up to 12 months. Avoid repeated freeze/thaw cycles.

Autres remarques

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

Informations légales

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

Clause de non-responsabilité

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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Réf. du produit
Description
Tarif

Pictogrammes

Health hazard
GHS08

Mention d'avertissement

Danger

Mentions de danger

H360FD

Classification des risques

Repr. 1B

Code de la classe de stockage

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Samantha L Hersrud et al.
The FEBS journal, 283(3), 459-471 (2015-11-14)
The neuronal ceroid lipofuscinoses (NCLs) are a group of neurodegenerative genetic diseases that primarily affect children and have no known cure. A unified clinical rating scale for the juvenile form of NCL has been developed, although it has not been
Chera L Maarouf et al.
PloS one, 6(11), e27291-e27291 (2011-11-17)
The amyloid cascade hypothesis provides an economical mechanistic explanation for Alzheimer's disease (AD) dementia and correlated neuropathology. However, some nonagenarian individuals (high pathology controls, HPC) remain cognitively intact while enduring high amyloid plaque loads for decades. If amyloid accumulation is
Chera L Maarouf et al.
PloS one, 9(8), e105784-e105784 (2014-08-29)
Defining the biochemical alterations that occur in the brain during "normal" aging is an important part of understanding the pathophysiology of neurodegenerative diseases and of distinguishing pathological conditions from aging-associated changes. Three groups were selected based on age and on

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