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MAB1308

Sigma-Aldrich

Mouse Anti-Human IgG2 Antibody, clone HP6002, Fc

clone HP6002, Chemicon®, from mouse

Synonyme(s) :

Anti-Anti-CD32, Anti-Anti-CD32B, Anti-Anti-FCG2, Anti-Anti-FCGR2, Anti-Anti-FCGR2C, Anti-Anti-FcGRIIB, Anti-Anti-FcRII-c, Anti-Anti-FcgammaRIIb, Anti-Anti-IGFR2

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About This Item

Code UNSPSC :
12352203
eCl@ss :
32160702
Nomenclature NACRES :
NA.46

Source biologique

mouse

Niveau de qualité

100

Forme d'anticorps

purified immunoglobulin

Type de produit anticorps

secondary antibodies

Clone

HP6002, monoclonal

Espèces réactives

human

Fabricant/nom de marque

Chemicon®

Technique(s)

ELISA: suitable
radioimmunoassay: suitable
western blot: suitable

Isotype

IgG1

Numéro d'accès NCBI

NM_001002273.1
NM_001002274.1
NM_001002275.1
NM_004001.3

Numéro d'accès UniProt

P31994

Conditions d'expédition

wet ice

Modification post-traductionnelle de la cible

unmodified

Informations sur le gène

human ... FCGR2B(2213)

Catégories apparentées

Spécificité

Human IgG2 Fc. ELISA Specificity: (Hamilton et al., 1987) human IgG subclass 1-0.02% human IgG subclass 2- 100% human IgG subclass 3- 0.01%

human IgG subclass 4- 0.01% Isoelectric Focusing: mean pI 7.1

Application

This Mouse anti-Human IgG2 Antibody, clone HP6002, Fc is validated for use in ELISA, RIA, WB for the detection of Human IgG2.
This antibody employed as both a capture antibody and a detection antibody for human IgG2 in enzyme linked immunosorbent assays, radio-immunoassay and EIA affinity immunoblots (Papadea et al., 1985; Hamilton, et al., 1987).

Final working dilutions must be determined by end user.

Liaison

Replaces: 411462-200UG

Forme physique

Format: Purified
Purified Immunoglobulin. Liquid in 0.02M Phosphate buffer, pH=7.6, 0.25M NaCl containing 0.1% sodium azide.

Stockage et stabilité

Maintain at 2-8°C for up to one year in undiluted aliquots.

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

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Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 2

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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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Corine G Demanga et al.
Infection and immunity, 78(1), 486-494 (2009-11-04)
Plasmodium falciparum merozoite surface protein (MSP3) is a main target of protective immunity against malaria that is currently undergoing vaccine development. It was shown recently to belong, together with MSP6, to a new multigene family whose C-terminal regions have a
Subhash Singh et al.
The Journal of infectious diseases, 190(5), 1010-1018 (2004-08-06)
Merozoite surface protein 3 (MSP3) is a target of antibody-dependent cellular inhibition (ADCI), a protective mechanism against Plasmodium falciparum malaria. From the C-terminal half of the molecule, 6 overlapping peptides were chosen to characterize human immune responses. Each peptide defined
Suzanne E Barbour et al.
Infection and immunity, 70(6), 2780-2786 (2002-05-16)
Several lines of evidence indicate that the monocytes of subjects with localized juvenile periodontitis (LJP) are functionally distinct from cells of age- and race-matched nonperiodontitis (NP) subjects. Among the abnormalities are the propensity to secrete large amounts of prostaglandin E(2)
Elizabeth H Aitken et al.
eLife, 10 (2021-06-29)
Plasmodium falciparum causes placental malaria, which results in adverse outcomes for mother and child. P. falciparum-infected erythrocytes that express the parasite protein VAR2CSA on their surface can bind to placental chondroitin sulfate A. It has been hypothesized that naturally acquired
Katherine A McLaughlin et al.
Journal of immunology (Baltimore, Md. : 1950), 183(6), 4067-4076 (2009-08-19)
Multiple sclerosis (MS) typically manifests in early to mid adulthood, but there is increasing recognition of pediatric-onset MS, aided by improvements in imaging techniques. The immunological mechanisms of disease are largely unexplored in pediatric-onset MS, in part because studies have
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