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Invitrogen™ MTM1 Polyclonal Antibody
Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA587393
Description
Immunogen sequence: SARERQKVTE RTVSLWSLIN SNKEKFKNPF YTKEINRVLY PVASMRHLEL WVNYYIRWNP RIKQQQPNPV EQRYMELLAL RDEYIKRLEE LQLANSAKLS DPPTSPSSPS QMMPHVQTHF; Positive Samples: Mouse liver, NCI-H460; Cellular Location: Cell membrane, Cell projection, Cytoplasm, Late endosome, Peripheral membrane protein, filopodium, ruffle.
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.
Specifications
MTM1 | |
Polyclonal | |
Unconjugated | |
MTM1 | |
AF073996; CG2; CNM; fb19c01; hypothetical protein LOC560881; im:6903724; mKIAA4176; Mtm; MTM1; MTMX; myotubularin; myotubularin 1; Myotubularin-like protein; phosphatidylinositol-3,5-bisphosphate 3-phosphatase; Phosphatidylinositol-3-phosphate phosphatase; wu:fb19c01; X-linked myotubular myopathy gene 1; XLMTM; zgc:123266 | |
Rabbit | |
Affinity Chromatography | |
RUO | |
17772, 4534 | |
-20°C, Avoid Freeze/Thaw Cycles | |
Liquid |
ELISA, Western Blot | |
1.45 mg/mL | |
PBS with 50% glycerol and 0.02% sodium azide; pH 7.3 | |
Q13496, Q9Z2C5 | |
MTM1 | |
Recombinant fusion protein containing a sequence corresponding to amino acids 484-603 of human MTM1 (NP_0002431). | |
100 μL | |
Primary | |
Human, Mouse | |
Antibody | |
IgG |
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