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MABS442

Sigma-Aldrich

Anti-Myotubularin Antibody, clone 1G6

ascites fluid, clone 1G6, from mouse

Sinônimo(s):

Myotubularin

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About This Item

Código UNSPSC:
12352203
eCl@ss:
32160702
NACRES:
NA.41

fonte biológica

mouse

Nível de qualidade

forma do anticorpo

ascites fluid

tipo de produto de anticorpo

primary antibodies

clone

1G6, monoclonal

reatividade de espécies

mouse, yeast, human

técnica(s)

immunocytochemistry: suitable
immunoprecipitation (IP): suitable
western blot: suitable

Isotipo

IgG1κ

nº de adesão NCBI

nº de adesão UniProt

Condições de expedição

wet ice

modificação pós-traducional do alvo

unmodified

Informações sobre genes

human ... MTM1(4534)

Descrição geral

Myotubularin is a cytoplasmic phosphatase which belongs to the protein-tyrosine phosphatase family. It contains a GRAM domain and a myotubularin phosphatase domain. Myotubularin targets phosphoinositide substrates, including phosphatidylinositol 3-monophosphate (PI3P) and phosphatidylinositol 3,5-bisphosphate (PI(3,5)P2). It may also dephosphorylate phosphotyrosine- and phosphoserine-containing peptides. Myotubularin indirectly regulates many cellular processes that are facilitated by phosphoinositides, and plays an important role in the formation and morphology of membrane-bound intracellular structures such as vacuoles and mitochondria. It also regulates the transport of EGFR from late endosomes to lysosomes, resulting in the degradation of EGFR. Defects in myotubularin result in X-linked myotubular myopathy, a congenital muscle-wasting condition that affects the limb girdle, trunk, and neck muscles. It has also been implicated in other neuromuscular diseases, such as Charcot-Marie-Tooth disease type 4B.

Imunogênio

Epitope: N-terminus
Ovalbumin-conjugated recombinant protein corresponding to the N-terminus of human Myotubularin.

Aplicação

Research Category
Signaling
Research Sub Category
Signaling Neuroscience
This Anti-Myotubularin Antibody, clone 1G6 is validated for use in western blotting, ICC & IP for the detection of Myotubularin.
Western Blotting Analysis: A 1:1,000 dilution from a representative lot detected Myotubularin in 10 µg of HL-60 cell lysate.

Western Blotting Analysis: A representative lot from an independent laboratory detected Myotubularin in lymphoblast lysates (Laporte, J., et al. (2002). J Cell Sci. 115(Pt 15):3105-3117.).

Immunoprecipitation Analysis: A representative lot from an independent laboratory immunoprecipitated Myotubularin from C2C12 cell lysates. (Laporte, J., et al. (2002). J Cell Sci. 115(Pt 15):3105-3117.).

Immunocytochemistry Analysis: A representative lot from an independent laboratory detected Myotubularin from C2C12 cells. (Buj-Bello, A. et al. (2002). Hum Mol Genet. 11(19):2297-2307.).

Qualidade

Evaluated by Western Blotting in HeLa cell lysate.

Western Blotting Analysis: A 1:1,000 dilution of this antibody detected Myotubularin in 10 µg of HeLa cell lysate.

Descrição-alvo

~70 kDa observed

forma física

Mouse monoclonal IgG1κ in ascites without preservatives.
Unpurified

Armazenamento e estabilidade

Stable for 1 year at -20°C from date of receipt.
Handling Recommendations: Upon receipt and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.

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 1

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable


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Jocelyn Laporte et al.
Journal of cell science, 115(Pt 15), 3105-3117 (2002-07-16)
Myotubularin, the phosphatase mutated in X-linked myotubular myopathy, was shown to dephosphorylate phosphatidylinositol 3-monophosphate (PtdIns3P) and was also reported to interact with nuclear transcriptional regulators from the trithorax family. We have characterized a panel of specific antibodies and investigated the
Anna Buj-Bello et al.
Human molecular genetics, 11(19), 2297-2307 (2002-09-10)
The myotubularin-related 1 (MTMR1) gene belongs to a highly conserved family of eucaryotic phosphatases, with at least 11 members in humans. The founder member of this gene family, MTM1, is mutated in X-linked myotubular myopathy, a severe congenital disorder that

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