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401253

Sigma-Aldrich

Goat Anti-Mouse IgG, H&L Chain Specific Peroxidase Conjugate

liquid, Calbiochem®

Synonyme(s) :

Anti-Mouse IgG Peroxidase

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About This Item

Code UNSPSC :
12352203
Nomenclature NACRES :
NA.46

Source biologique

goat

Niveau de qualité

Forme d'anticorps

affinity isolated antibody

Type de produit anticorps

secondary antibodies

Clone

polyclonal

Forme

liquid

Contient

0.02% thimerosal as preservative

Fabricant/nom de marque

Calbiochem®

Conditions de stockage

do not freeze

Isotype

IgG

Conditions d'expédition

wet ice

Température de stockage

2-8°C

Modification post-traductionnelle de la cible

unmodified

Description générale

Adsorbed against bovine, horse, and human serum proteins.
Immunoaffinity purified goat polyclonal antibody conjugated to horseradish peroxidase. Adsorbed against bovine, horse, and human serum proteins. Recognizes mouse IgG, heavy and light chains.
This Goat Anti-Mouse IgG, H&L Chain Specific Peroxidase Conjugate is validated for use in Enzyme Immunoassay, Immunoelectrophoresis for the detection of Mouse IgG, H&L Chain Specific.

Immunogène

Mouse

Application

Enzyme Immunoassay (1:10,000)

Immunoelectrophoresis (see comments)

Avertissement

Toxicity: Standard Handling (A)

Forme physique

In 10 mM PBS, 0.5 mM EDTA, 10% mannose, 2% sucrose, 1% BSA, pH 7.6.

Autres remarques

Monospecific for mouse IgG, heavy and light chains, as determined by immunoelectrophoresis against normal mouse serum. Cross-reactivity to normal bovine, horse and human sera: <1% by direct solid phase immunoassay. Variables associated with assay conditions will dictate the proper working dilution.

Informations légales

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

Clause de non-responsabilité

To comply with ban of sale of mercury-added products required by The Interstate Mercury Education and Reduction Clearinghouse (IMERC), this product is prohibited to be sold in the following US states: Rhode Island and Connecticut.

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Code de la classe de stockage

12 - Non 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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Consulter la Bibliothèque de documents

Rocco Bernasconi et al.
EMBO molecular medicine, 13(10), e14392-e14392 (2021-08-31)
Recessive dystrophic epidermolysis bullosa (RDEB), a genetic skin blistering disease, is a paradigmatic condition of tissue fragility-driven multi-organ fibrosis. Here, longitudinal analyses of the tissue proteome through the course of naturally developing disease in RDEB mice revealed that increased pro-inflammatory
Frances E Carr et al.
Endocrinology, 157(8), 3278-3292 (2016-06-03)
Dysregulation of the thyroid hormone receptor (TR)β is common in human cancers. Restoration of functional TRβ delays tumor progression in models of thyroid and breast cancers implicating TRβ as a tumor suppressor. Conversely, aberrant expression of the runt-related transcription factor
Liang-yan Xue et al.
Oncogene, 22(58), 9197-9204 (2003-12-19)
The antiapoptotic oncoprotein Bcl-2 is now a recognized phototarget of photodynamic therapy (PDT) with the phthalocyanine Pc 4 and with other mitochondrion-targeting photosensitizers. Photodamage, observed on Western blots as the loss of the native 26-kDa Bcl-2 protein, is PDT dose
Margarida Barroso et al.
The Journal of biological chemistry, 290(45), 27101-27112 (2015-09-25)
Antigen processing and MHC class II-restricted antigen presentation by antigen-presenting cells such as dendritic cells and B cells allows the activation of naïve CD4+ T cells and cognate interactions between B cells and effector CD4+ T cells, respectively. B cells
Cheng Cheng et al.
Cell reports, 25(6), 1404-1414 (2018-11-08)
Mutations of the transcriptional regulator PHF6 cause the X-linked intellectual disability disorder Börjeson-Forssman-Lehmann syndrome (BFLS), but the pathogenesis of BFLS remains poorly understood. Here, we report a mouse model of BFLS, generated using a CRISPR-Cas9 approach, in which cysteine 99

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