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Merck

SAB1102826

Sigma-Aldrich

Anti-TM4SF19 (146-160) antibody produced in rabbit

IgG fraction of antiserum

Synonym(e):

Anti-OCTM4, Anti-Transmembrane 4 L six family member 19

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About This Item

UNSPSC-Code:
12352203
NACRES:
NA.41

Biologische Quelle

rabbit

Konjugat

unconjugated

Antikörperform

IgG fraction of antiserum

Antikörper-Produkttyp

primary antibodies

Klon

polyclonal

Form

buffered aqueous solution

Mol-Gew.

antigen ~22 kDa

Speziesreaktivität

human

Methode(n)

western blot: 1:500-1:2,000

UniProt-Hinterlegungsnummer

Versandbedingung

dry ice

Lagertemp.

−20°C

Posttranslationale Modifikation Target

unmodified

Angaben zum Gen

Allgemeine Beschreibung

Transmembrane 4 L six family member 19 (TM4SF19) or osteoclast maturation-associated gene 4 protein (OCTM4) belongs to the transmembrane 4 L six superfamily. TM4SF19 gene is mapped to human chromosome 3q29.

Immunogen

synthetic peptide corresponding to amino acids 146-160 of human TM4SF19

Biochem./physiol. Wirkung

Transmembrane 4 L six family member 19 (TM4SF19) expression is detected in the chronic heart disease samples especially in the cells, sera and tissues. It may contribute to atherosclerosis progression and may serve as a potential marker for screening atherosclerosis.

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

12 - Non Combustible Liquids

WGK

WGK 2

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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Die Dokumentenbibliothek aufrufen

Adela Chirita Emandi et al.
Frontiers in pediatrics, 7, 270-270 (2019-07-25)
3q29 deletion syndrome is a rare disorder, causing a complex phenotype. Clinical features are variable and relatively non-specific. Our report aims to present an atypical, de novo deletion in chromosome band 3q29 in a preschool boy, first child of healthy
Yuji Kubota et al.
Nature communications, 13(1), 4063-4063 (2022-07-14)
Point-mutations of MEK1, a central component of ERK signaling, are present in cancer and RASopathies, but their precise biological effects remain obscure. Here, we report a mutant MEK1 structure that uncovers the mechanisms underlying abnormal activities of cancer- and RASopathy-associated
Li Ding et al.
Biochemical and biophysical research communications, 533(4), 1204-1211 (2020-10-17)
Atherosclerosis is a chronic vascular inflammatory disease that initially starts from an arterial intima lesion and endothelial barrier dysfunction. The purpose of this study was to investigate the role of TM4SF19, a recently identified member of the transmembrane 4L six

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