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MTM1 Produkte

(Myotubularin 1 (MTM1))

Kategorien

This gene encodes a dual-specificity phosphatase that acts on both phosphotyrosine and phosphoserine. It is required for muscle cell differentiation and mutations in this gene have been identified as being responsible for X-linked myotubular myopathy. [provided by RefSeq, Jul 2008].

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Ausgewählte MTM1 Kategorien

MTM1 Antikörper

High quality antibodies with extensive validation data.

MTM1 ELISA Kits

Reliable ELISA kits for a wide range of species.

MTM1 Proteine

Proteins for various applications incl. WB, ELISA, IF etc.

Empfohlene MTM1 Antikörper

Produkt
Reaktivität
Applikation
Validierungen
Kat. Nr.
Menge
Datenblatt
Reaktivität Human
Applikation WB, ELISA, IHC (p), RNAi
Validierungen
  • (1)
  • (5)
Kat. Nr. ABIN561867
Menge 100 μg
Datenblatt Datenblatt
Reaktivität Human, Mouse
Applikation WB, ELISA, IHC
Validierungen
  • (5)
Kat. Nr. ABIN184636
Menge 100 μg
Datenblatt Datenblatt
Reaktivität Human
Applikation WB
Validierungen
  • (4)
Kat. Nr. ABIN518078
Menge 100 μg
Datenblatt Datenblatt

Empfohlene MTM1 ELISA Kits

Produkt
Reaktivität
Analytical Method
Validierungen
Kat. Nr.
Menge
Datenblatt
Reaktivität Mouse
Analytical Method Quantitative Sandwich ELISA
Validierungen
Kat. Nr. ABIN5592364
Menge 96 tests
Datenblatt Datenblatt
Reaktivität Human
Analytical Method Quantitative Sandwich ELISA
Validierungen
Kat. Nr. ABIN5592363
Menge 96 tests
Datenblatt Datenblatt
Reaktivität Rat
Analytical Method
Validierungen
Kat. Nr. ABIN2869990
Menge 96 tests
Datenblatt Datenblatt

Empfohlene MTM1 Proteine

Produkt
Reaktivität
Source
Validierungen
Kat. Nr.
Menge
Datenblatt
Reaktivität Mouse
Source Tobacco (Nicotiana tabacum)
Validierungen
  • (3)
Kat. Nr. ABIN3137632
Menge 1 mg
Datenblatt Datenblatt
Reaktivität Human
Source Wheat germ
Validierungen
  • (1)
Kat. Nr. ABIN1311572
Menge 10 μg
Datenblatt Datenblatt
Reaktivität Human
Source Wheat germ
Validierungen
  • (1)
Kat. Nr. ABIN1781341
Menge 10 μg
Datenblatt Datenblatt

Neueste Publikationen zu unseren MTM1 Produkten

Agrawal, Pierson, Joshi, Liu, Ravenscroft, Moghadaszadeh, Talabere, Viola, Swanson, Haliloğlu, Talim, Yau, Allcock, Laing, Perrella, Beggs: "SPEG interacts with myotubularin, and its deficiency causes centronuclear myopathy with dilated cardiomyopathy." in: American journal of human genetics, Vol. 95, Issue 2, pp. 218-26, (2014) (PubMed).

Gupta, Hnia, Smith, Gundry, McIntire, Shimazu, Bass, Talbot, Amoasii, Goldman, Laporte, Beggs: "Loss of catalytically inactive lipid phosphatase myotubularin-related protein 12 impairs myotubularin stability and promotes centronuclear myopathy in zebrafish." in: PLoS genetics, Vol. 9, Issue 6, pp. e1003583, (2013) (PubMed).

Hedberg, Lindberg, Máthé, Moslemi, Oldfors: "Myopathy in a woman and her daughter associated with a novel splice site MTM1 mutation." in: Neuromuscular disorders : NMD, Vol. 22, Issue 3, pp. 244-51, (2012) (PubMed).

Jian, Cheng, Jiang, Deng, Hu, Zhang: "A cDNA-based random RNA interference library for functional genetic screens in embryonic stem cells." in: Stem cells (Dayton, Ohio), Vol. 25, Issue 8, pp. 1904-12, (2007) (PubMed).

Nandurkar, Layton, Laporte, Selan, Corcoran, Caldwell, Mochizuki, Majerus, Mitchell: "Identification of myotubularin as the lipid phosphatase catalytic subunit associated with the 3-phosphatase adapter protein, 3-PAP." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 100, Issue 15, pp. 8660-5, (2003) (PubMed).

Biancalana, Caron, Gallati, Baas, Kress, Novelli, DApice, Lagier-Tourenne, Buj-Bello, Romero, Mandel: "Characterisation of mutations in 77 patients with X-linked myotubular myopathy, including a family with a very mild phenotype." in: Human genetics, Vol. 112, Issue 2, pp. 135-42, (2003) (PubMed).

Herman, Kopacz, Zhao, Mills, Metzenberg, Das: "Characterization of mutations in fifty North American patients with X-linked myotubular myopathy." in: Human mutation, Vol. 19, Issue 2, pp. 114-21, (2002) (PubMed).

Wishart, Dixon: "PTEN and myotubularin phosphatases: from 3-phosphoinositide dephosphorylation to disease." in: Trends in cell biology, Vol. 12, Issue 12, pp. 579-85, (2002) (PubMed).

Sutton, Winer, Norman, Liechti-Gallati, MacDonald: "Limb girdle and facial weakness in female carriers of X-linked myotubular myopathy mutations." in: Neurology, Vol. 57, Issue 5, pp. 900-2, (2001) (PubMed).

Laporte, Hu, Kretz, Mandel, Kioschis, Coy, Klauck, Poustka, Dahl: "A gene mutated in X-linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeast." in: Nature genetics, Vol. 13, Issue 2, pp. 175-82, (1996) (PubMed).

Synonyme und alternative Namen zu MTM1

myotubularin 1 (MTM1), myotubularin 1 (mtm1), myotubularin 1 S homeolog (mtm1.S), myotubularin 1 (Mtm1), CNM, MTMX, wu:fb19c01, XLMTM, zgc:123266

Bezeichner auf Proteinebene für MTM1

  • myotubularin
  • myotubularin 1
  • fb19c01
  • myotubularin-like
  • X-linked myotubular myopathy gene 1
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