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MTMR2 antibody (N-Term)

The Rabbit Polyclonal anti-MTMR2 antibody has been validated for WB, FACS, IF and ICC. It is suitable to detect MTMR2 in samples from Human, Mouse and Rat.
Catalog No. ABIN7603228

Quick Overview for MTMR2 antibody (N-Term) (ABIN7603228)

Target

See all MTMR2 Antibodies
MTMR2 (Myotubularin Related Protein 2 (MTMR2))

Reactivity

Human, Mouse, Rat

Host

  • 26
  • 2
Rabbit

Clonality

  • 26
  • 2
Polyclonal

Conjugate

  • 10
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This MTMR2 antibody is un-conjugated

Application

  • 24
  • 13
  • 13
  • 10
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Flow Cytometry (FACS), Immunofluorescence (IF), Immunocytochemistry (ICC)
  • Binding Specificity

    • 15
    • 6
    • 1
    • 1
    • 1
    • 1
    • 1
    N-Term

    Purpose

    Anti-MTMR2 Antibody Picoband®

    Cross-Reactivity (Details)

    No cross-reactivity with other proteins.

    Characteristics

    Anti-MTMR2 Antibody Picoband® (ABIN7603228). Tested in Flow Cytometry, IF, ICC, WB applications. This antibody reacts with Human, Mouse, Rat. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.

    Purification

    Immunogen affinity purified.

    Immunogen

    A synthetic peptide corresponding to a sequence at the N-terminus of human MTMR2, identical to the related mouse sequences.

    Isotype

    IgG
  • Application Notes

    Western blot, 0.25-0.5 μg/mL, Human, Mouse, Rat
    Immunocytochemistry/Immunofluorescence, 5 μg/mL, Human
    Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
    1. Begley, M. J., Taylor, G. S., Brock, M. A., Ghosh, P., Woods, V. L., Dixon, J. E. Molecular basis for substrate recognition by MTMR2, a myotubularin family phosphoinositide phosphatase. Proc. Nat. Acad. Sci. 103: 927-932, 2006. 2. Berger, P., Bonneick, S., Willi, S., Wymann, M., Suter, U. Loss of phosphatase activity in myotubularin-related protein 2 is associated with Charcot-Marie-Tooth disease type 4B1. Hum. Molec. Genet. 11: 1569-1579, 2002. 3. Berger, P., Schaffitzel, C., Berger, I., Ban, N., Suter, U. Membrane association of myotubularin-related protein 2 is mediated by a pleckstrin homology-GRAM domain and a coiled-coil dimerization module. Proc. Nat. Acad. Sci. 100: 12177-12182, 2003.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    Concentration

    500 μg/mL

    Buffer

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

    Storage

    4 °C,-20 °C

    Storage Comment

    At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
  • Target

    MTMR2 (Myotubularin Related Protein 2 (MTMR2))

    Alternative Name

    MTMR2

    Background

    Synonyms: Transforming acidic coiled-coil-containing protein 1,Gastric cancer antigen Ga55,Taxin-1,TACC1,KIAA1103,

    Tissue Specificity: Isoform 1, isoform 3 and isoform 5 are ubiquitous. Isoform 2 is strongly expressed in the brain, weakly detectable in lung and colon, and overexpressed in gastric cancer. Isoform 4 is not detected in normal tissues, but strong expression was found in gastric cancer tissues. Down-regulated in a subset of cases of breast cancer. .

    Background: Myotubularin-related protein 2 also known as phosphatidylinositol-3,5-bisphosphate 3-phosphatase or phosphatidylinositol-3-phosphate phosphatase is a protein that in humans is encoded by the MTMR2 gene. This gene is a member of the myotubularin family of phosphoinositide lipid phosphatases. The encoded protein possesses phosphatase activity towards phosphatidylinositol-3-phosphate and phosphatidylinositol-3,5-bisphosphate. Mutations in this gene are a cause of Charcot-Marie-Tooth disease type 4B, an autosomal recessive demyelinating neuropathy. Alternatively spliced transcript variants encoding multiple isoforms have been found for this gene.

    Molecular Weight

    73 kDa

    Gene ID

    8898

    UniProt

    Q13614

    Pathways

    Inositol Metabolic Process, Synaptic Membrane
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