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SAB4301475

Sigma-Aldrich

Anti-phospho-Calmodulin (pThr79/Ser81) antibody produced in rabbit

affinity isolated antibody

Sinonimo/i:

CALM, CALM1, CALM2, CALM3, CAM

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About This Item

Codice UNSPSC:
12352203
NACRES:
NA.41

Origine biologica

rabbit

Livello qualitativo

Forma dell’anticorpo

affinity isolated antibody

Tipo di anticorpo

primary antibodies

Clone

polyclonal

Forma fisica

buffered aqueous solution

PM

17 kDa

Reattività contro le specie

rat, mouse, human

Concentrazione

1.0 mg/mL

tecniche

western blot: 1:500-1:1000 (Cell Lysate)

Isotipo

IgG

Numero d’accesso

NP_005175.2

N° accesso UniProt

Condizioni di spedizione

wet ice

Temperatura di conservazione

−20°C

modifica post-traduzionali bersaglio

phosphorylation (pThr79)

Informazioni sul gene

human ... CALM3(808)

Descrizione generale

Calmodulin 3 (CALM3) encodes calmodulin (CaM) protein 3 which is expressed five folds more than CALM1 and CALM2. CALM3 promoter has high GC content and no TATA box like that of housekeeping gene. CALM3 contains several pro-alpha1 (AP1) and pro-alpha2 (AP2) consensus sites and several CAAT regions. CALM3 also has clusters of specificity protein 1 (SP1) transcription factor. In human chromosome, the gene is localized on 19q13.32.

Specificità

The antibody detects endogenous level of Calmodulin only when phosphorylated at threonine 79/serine 81.

Immunogeno

Peptide sequence around phosphorylation site of threonine79/serine81(K-D-T(p)-D-S(p)-E-E) derived from Human Calmodulin .

Azioni biochim/fisiol

Calmodulin (CaM) encoded by Calmodulin 3 (CALM3) senses Ca2+ and binds to free signal-transducing protein that regulates Cav1.2 L-type calcium channel and deactivates Cav1.2 when CaM binds to free Ca2+. A sporadic mutation in CALM3 might be the cause for long QT syndrome, a disorder of ventricular myocardial repolarization, characterized by prolonged heart rate. CALM3 expression is higher in teratoma cells. CALM3 is a potential biomarker to dysregulate the melanoma cancer genes. Polymorphism in CALM3 is a potential modifier gene for familial hypertrophic cardiomyopathy.

Caratteristiche e vantaggi

Evaluate our antibodies with complete peace of mind. If the antibody does not perform in your application, we will issue a full credit or replacement antibody. Learn more.

Stato fisico

Rabbit IgG in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.

Esclusione di responsabilità

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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Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


Certificati d'analisi (COA)

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Tumour-suppressive microRNA-224 inhibits cancer cell migration and invasion via targeting oncogenic TPD52 in prostate cancer
Goto Y, et al.
Febs Letters, 588(10), 1973-1982 (2014)
Characterization of the human CALM2 calmodulin gene and comparison of the transcriptional activity of CALM1, CALM2 and CALMS
Toutenhoofd SL, et al.
Cell Calcium, 23(5), 323-338 (1998)
Identification of melanoma biomarkers based on network modules by integrating the human signalling network with microarrays
Huang C, et al.
Journal of Cancer Research and Therapeutics, 10(7), 114-124 (2014)
A new polymorphism in human calmodulin III gene promoter is a potential modifier gene for familial hypertrophic cardiomyopathy
Friedrich FW, et al.
European Heart Journal, 30(13), 1648-1655 (2009)
CALM3 mutation associated with long QT syndrome
Reed GJ, et al.
Heart Rhythm : the Official Journal of the Heart Rhythm Society, 12(2), 419-422 (2015)

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