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MAB1548

Sigma-Aldrich

Anti-Myosin Antibody, heavy chain β

culture supernatant, clone 5B9 (2C8), Chemicon®

Synonym(e):

Anti-CMD1S, Anti-MPD1, Anti-MYHCB, Anti-SPMD, Anti-SPMM

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About This Item

UNSPSC-Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41

Biologische Quelle

mouse

Qualitätsniveau

100

Antikörperform

culture supernatant

Antikörper-Produkttyp

primary antibodies

Klon

5B9 (2C8), monoclonal

Speziesreaktivität

human

Hersteller/Markenname

Chemicon®

Methode(n)

immunohistochemistry: suitable
western blot: suitable

Isotyp

IgG2a

NCBI-Hinterlegungsnummer

NM_000257.2

UniProt-Hinterlegungsnummer

P12883

Versandbedingung

wet ice

Posttranslationale Modifikation Target

unmodified

Angaben zum Gen

rat ... Myh7(29557)

Spezifität

Recognizes the S1/S2 junction of human ventricular myosin heavy chain beta

Immunogen

Epitope: heavy chain beta
Human ventricular myosin

Anwendung

Detect Myosin using this Anti-Myosin Antibody, heavy chain β validated for use in WB, IH.
Immunohistochemistry: Neat (undiluted)
Western blot: 1:10

Optimal dilutions must be determined by the end user.

Physikalische Form

Supernatant in RPMI 1640, 10% FCS, 0.01% sodium azide.

Lagerung und Haltbarkeit

Maintain at -20°C in undiluted aliquots for up to 12 months. Avoid repeated freeze/thaw cycles.

Rechtliche Hinweise

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

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Lagerklassenschlüssel

12 - Non Combustible Liquids

WGK

WGK 2

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Henry E Young et al.
The anatomical record. Part A, Discoveries in molecular, cellular, and evolutionary biology, 276(1), 75-102 (2003-12-31)
Development of a multicellular organism is accomplished through a series of events that are preprogrammed in the genome. These events encompass cellular proliferation, lineage commitment, lineage progression, lineage expression, cellular inhibition, and regulated apoptosis. The sequential progression of cells through
Siva K Panguluri et al.
American journal of physiology. Heart and circulatory physiology, 304(12), H1651-H1661 (2013-04-16)
Ventricular arrhythmias account for high mortality in cardiopulmonary patients in intensive care units. Cardiovascular alterations and molecular-level changes in response to the commonly used oxygen treatment remains unknown. In the present study we investigated cardiac hypertrophy and cardiac complications in
Barbara S Mallon et al.
Stem cell research, 12(2), 376-386 (2014-01-01)
Many studies have compared the genetic and epigenetic profiles of human induced pluripotent stem cells (hiPSCs) to human embryonic stem cells (hESCs) and yet the picture remains unclear. To address this, we derived a population of neural precursor cells (NPCs)
Henry E Young et al.
The anatomical record. Part A, Discoveries in molecular, cellular, and evolutionary biology, 277(1), 178-203 (2004-02-26)
Undifferentiated cells have been identified in the prenatal blastocyst, inner cell mass, and gonadal ridges of rodents and primates, including humans. After isolation these cells express molecular and immunological markers for embryonic cells, capabilities for extended self-renewal, and telomerase activity.
Richard P Davis et al.
Circulation, 125(25), 3079-3091 (2012-06-01)
Pluripotent stem cells (PSCs) offer a new paradigm for modeling genetic cardiac diseases, but it is unclear whether mouse and human PSCs can truly model both gain- and loss-of-function genetic disorders affecting the Na(+) current (I(Na)) because of the immaturity
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