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Merck

SAB4200728

Sigma-Aldrich

Anti-Chromogranin-A antibody, Mouse monoclonal

clone CHGA(419), purified from hybridoma cell culture

Synonym(e):

Anti-CHGA, Anti-CgA, Anti-Pituitary secretory protein I, Anti-SP-1

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About This Item

UNSPSC-Code:
41116158
NACRES:
NA.41

Biologische Quelle

mouse

Antikörperform

purified from hybridoma cell culture

Antikörper-Produkttyp

primary antibodies

Klon

CHGA(419), monoclonal

Form

buffered aqueous solution

Mol-Gew.

~50 kDa

Speziesreaktivität

human

Konzentration

~1.0 mg/mL

Methode(n)

immunoblotting: 10-20 μg/mL using human embryonic kidney 293T cell extract
immunohistochemistry: 10-20 μg/mL using heat-retrieved formalin-fixed, paraffin-embedded Human Stomach sections

Isotyp

IgG1

UniProt-Hinterlegungsnummer

Versandbedingung

dry ice

Lagertemp.

−20°C

Posttranslationale Modifikation Target

unmodified

Angaben zum Gen

human ... CHGA(1113)

Allgemeine Beschreibung

Anti-Chromogranin-A antibody, Mouse monoclonal (mouse IgG1 isotype) is derived from the CHGA(419) hybridoma produced by the fusion of mouse myeloma cells and splenocytes from a BALB/c mouse immunized with synthetic peptide corresponding to the C-terminal region of human Chromogranin-A protein, conjugated to KLH. Chromogranin-A protein, also known as CgA, pituitary secretory protein I (SP-1) is the major member of the granin family of acidic secretory glycoproteins that are expressed in all endocrine and neuroendocrine cells. The protein is in neuroendocrine cells distributed throughout the body, including the neuroendocrine cells of the large and small intestine, adrenal medulla and pancreatic islets and the secretory vesicles of neurons.

Immunogen

synthetic peptide corresponding to the C-terminal region of human Chromogranin-A protein conjugated to KLH

Anwendung

Anti-Chromogranin-A antibody has been used in immunohistochemistry,immunoblotting.

Biochem./physiol. Wirkung

Chromogranin-A has a crucial intracellular role in secretory granule biogenesis and calcium homeostasis. Tissue-specific and context-specific proteolytic cleavage of Chromogranin-A yields polypeptides with paracrine and endocrine activity including: vasostatin, catestatin, GE25 and WE-14. Increased blood levels of Chromogranin-A have been shown in numerous inflammatory and non-inflammatory conditions, including neuroendocrine tumours (carcinoid tumors, phenochromocytomas, paragangliomas and others), renal failure, arterial hypertension, chronic heart failure and rheumatoid arthritis.

Physikalische Form

Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.

Haftungsausschluss

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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Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 1

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


Analysenzertifikate (COA)

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Die Dokumentenbibliothek aufrufen

A new human chromogranin A (CgA) immunoradiometric assay involving monoclonal antibodies raised against the unprocessed central domain (145-245)
Degorce F, et al.
British Journal of Cancer, 79(1), 65-65 (1999)
Chromogranin A: its clinical value as marker of neuroendocrine tumours.
Nobels FR, et al.
European Journal of Clinical Investigation, 28(6), 431-440 (1998)
Chromogranin-A production and fragmentation in patients with Takayasu arteritis
Tombetti E, et al.
Arthritis Research & Therapy, 18(1), 187-187 (2016)
The endocrine role for chromogranin A: a prohormone for peptides with regulatory properties
Helle KB, et al.
Cellular and Molecular Life Sciences, 64(22), 2863-2886 (2007)
Gervaise H Henry et al.
Cell reports, 25(12), 3530-3542 (2018-12-20)
A comprehensive cellular anatomy of normal human prostate is essential for solving the cellular origins of benign prostatic hyperplasia and prostate cancer. The tools used to analyze the contribution of individual cell types are not robust. We provide a cellular

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