CBL66
Anti-Atrial Natriuretic Peptide Antibody, clone A6
clone A6, Chemicon®, from mouse
Sinônimo(s):
ANP
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About This Item
Código UNSPSC:
12352203
eCl@ss:
32160702
NACRES:
NA.41
Preço e disponibilidade não estão disponíveis no momento.
Produtos recomendados
fonte biológica
mouse
Nível de qualidade
forma do anticorpo
affinity purified immunoglobulin
tipo de produto de anticorpo
primary antibodies
clone
A6, monoclonal
reatividade de espécies
human
fabricante/nome comercial
Chemicon®
técnica(s)
immunohistochemistry: suitable (paraffin)
radioimmunoassay: suitable
Isotipo
IgG1
nº de adesão NCBI
nº de adesão UniProt
Condições de expedição
wet ice
Informações sobre genes
human ... NPPA(4878)
Especificidade
ANP (Whole molecule and residues 4-28)
FUSION PARTNER: NSO myeloma cell line
FUSION PARTNER: NSO myeloma cell line
Imunogênio
ANP/BSA conjugate
Aplicação
Competetive radioimmunoassay
(Clinical measurement of circulating ANP levels possibly in conjunction with cyclic GMP)
Liquid phase assay without plasma extraction
Staining of formalin-fixed wax embedded tissue
Optimal working dilutions must be determined by the end user.
(Clinical measurement of circulating ANP levels possibly in conjunction with cyclic GMP)
Liquid phase assay without plasma extraction
Staining of formalin-fixed wax embedded tissue
Optimal working dilutions must be determined by the end user.
Detect Atrial Natriuretic Peptide using this Anti-Atrial Natriuretic Peptide Antibody, clone A6 validated for use in IH(P), RIA.
Research Category
Neuroscience
Neuroscience
Research Sub Category
Hormones & Receptors
Hormones & Receptors
forma física
Format: Purified
The monoclonal is presented at a concentration of 1mg in phosphate buffered saline containing 10mM sodium azide. We recommend that each laboratory determine an optimum working titre for use in its particular application.
Armazenamento e estabilidade
For use within 1 month of purchase store at +4°C, for long term storage aliquot antibody into small volumes and store at -20°C.
Informações legais
CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany
Exoneração de responsabilidade
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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Código de classe de armazenamento
10 - Combustible liquids
Classe de risco de água (WGK)
WGK 2
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Certificados de análise (COA)
Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.
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Ultrastructural and immunocharacterization of undifferentiated myocardial cells in the developing mouse heart.
Zhang, F; Pasumarthi, KB
Journal of Cellular and Molecular Medicine null
E Farina-Lipari et al.
European journal of histochemistry : EJH, 47(2), 133-138 (2003-06-05)
In this work, we showed the presence of atrial natriuretic factor (ANF) in human prostate and compared its localisation in normal and hyperplastic conditions. ANF was localised in epithelial and stromal cells, being increased in hyperplasia, mainly in the stromal
Assessment of embryonic myocardial cell differentiation using a dual fluorescent reporter system.
McMullen, NM; Zhang, F; Pasumarthi, KB
Journal of Cellular and Molecular Medicine null
T V Sukhacheva et al.
Arkhiv patologii, 79(4), 3-12 (2017-08-10)
to analyze the morphological features of the myocardium of the atrial appendages in patients with different forms of atrial fibrillation (AF) and to compare the findings with the clinical parameters of patients. Light and electron microscopies were used to examine
Martijn Wehrens et al.
Cell reports, 39(6), 110809-110809 (2022-05-12)
Hypertrophic cardiomyopathy (HCM) is a genetic heart disease that is characterized by unexplained segmental hypertrophy that is usually most pronounced in the septum. While sarcomeric gene mutations are often the genetic basis for HCM, the mechanistic origin for the heterogeneous
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