Myotubularin (Y290) pAb

Cat no: BS2971

Supplier: Bioworld Technology, Inc.

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Human MTM1, a 603 amino-acid protein, is mutated in myotubular myopathy. The largely related protein hMTMR2 is found mutated in a recessive form of Charcot-Marie-tooth neuropathy. Myotubularin is primarily a lipid phosphatase that acts on hosphatidylinositol 3-monophosphate and is involved in the regulation of the phosphatidylinositol 3-kinase (PI 3-kinase) pathway and membrane trafficking. Wildtype myotubularin can directly dephosphorylate PI 3-P and PI 4-P in vitro. Thus, it decreases PI 3-P levels by down-regulating PI 3-K activity and by facilitating the degradation of PI 3-P.

Catalogue number:	BS2971
Reactivities:	Human, Mouse
Hosts:	Rabbit
Applications:	Western Blot
Size:	100ug/100ul
Swiss prot:	Q13496
Dilutions:	WB: 1:500~1:1000
Form:	liquid
Storage buffer:	1 mg/ml in Phosphate buffered saline (PBS) with 0.05% sodium azide, approx. pH 7.2.
Concentration:	1ug/ul
Antigen:	Synthetic peptide, corresponding to amino acids 256-3111 of Human Myotubularin.
Species:	Myotubularin (Y290) pAb detects endogenous levels of Myotubularin protein.
Molecular weight:	~ 70 kDa
Purity:	The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Storage temp:	Store at 4 degrees C short term. Aliquot and store at -20 degrees C long term. Avoid freeze-thaw cycles.
Alternative names:	AF073996; CG2; CNM; CNM; KIAA4176; mKIAA4176; Mtm; Mtm1; MTM1; MTMX; MTMX; Myotubular myopathy 1; Myotubular myopathy 1; Myotubularin; XLMTM; XLMTM;
Additional info:	For research use only, not for use in diagnostic procedure.

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Myotubularin (Y290) pAb

Cat no: BS2971

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