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POMT2 antibody

This anti-POMT2 antibody is a Rabbit Polyclonal antibody detecting POMT2 in WB, IHC, FACS, ICC and IF. Suitable for Human, Mouse and Rat.
Catalog No. ABIN6719505

Quick Overview for POMT2 antibody (ABIN6719505)

Target

See all POMT2 Antibodies
POMT2 (Protein-O-Mannosyltransferase 2 (POMT2))

Reactivity

  • 21
  • 8
  • 6
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 18
  • 3
Rabbit

Clonality

  • 19
  • 2
Polyclonal

Conjugate

  • 14
  • 2
  • 2
  • 1
  • 1
  • 1
This POMT2 antibody is un-conjugated

Application

Western Blotting (WB), Immunohistochemistry (IHC), Flow Cytometry (FACS), Immunocytochemistry (ICC), Immunofluorescence (IF)
  • Purpose

    Anti-POMT2 Antibody Picoband®

    Sequence

    QAARAAGRDV AAEAVARSPK R

    Cross-Reactivity (Details)

    No cross-reactivity with other proteins.

    Characteristics

    Anti-POMT2 Antibody Picoband® (ABIN6719505). Tested in Flow Cytometry, IF, IHC, 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 POMT2, which shares 61.9% amino acid (aa) sequence identity with both mouse and rat POMT2.

    Isotype

    IgG
  • Application Notes

    Western blot, 0.1-0.5 μg/mL
    Immunohistochemistry (Paraffin-embedded Section), 0.5-1 μg/mL
    Immunocytochemistry/Immunofluorescence, 2 μg/mL
    Flow Cytometry (Fixed), 1-3 μg/1x106 cells
    1. Biancheri, R., Falace, A., Tessa, A., Pedemonte, M., Scapolan, S., Cassandrini, D., Aiello, C., Rossi, A., Broda, P., Zara, F., Santorelli, F. M., Minetti, C., Bruno, C. POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changes. Biochem. Biophys. Res. Commun. 363: 1033-1037, 2007. 2. Mercuri, E., D'Amico, A., Tessa, A., Berardinelli, A., Pane, M., Messina, S., van Reeuwijk, J., Bertini, E., Muntoni, F., Santorelli, F. M. POMT2 mutation in a patient with 'MEB-like' phenotype. Neuromusc. Disord. 16: 446-448, 2006.

    Comment

    Tested Species: In-house tested species with positive results. By Heat: Boiling the paraffin sections in 10mM citrate buffer, pH6.0, for 20mins is required for the staining of formalin/paraffin sections. Other applications have not been tested. Optimal dilutions should be determined by end users.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 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, 0.05 mg Sodium azide.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store 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 freeze-thaw cycles.
  • Target

    POMT2 (Protein-O-Mannosyltransferase 2 (POMT2))

    Alternative Name

    POMT2

    Background

    Synonyms: Protein O-mannosyl-transferase 2, Dolichyl-phosphate-mannose--protein mannosyltransferase 2, POMT2

    Tissue Specificity: Highly expressed in testis, detected at low levels in most tissues.

    Background: Protein O-mannosyl-transferase 2 is an enzyme that in humans is encoded by the POMT2 gene. This gene is mapped to chromosome 14q24.3. The protein encoded by this gene is an O-mannosyltransferase that requires interaction with the product of the POMT1 gene for enzymatic function. The encoded protein is found in the membrane of the endoplasmic reticulum. Defects in this gene are a cause of Walker-Warburg syndrome (WWS).

    Molecular Weight

    84 kDa

    Gene ID

    29954
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