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MAGT1 antibody (N-Term)

The Rabbit Polyclonal anti-MAGT1 antibody has been validated for WB and FACS. It is suitable to detect MAGT1 in samples from Human and Mouse.
Catalog No. ABIN5536659

Quick Overview for MAGT1 antibody (N-Term) (ABIN5536659)

Target

See all MAGT1 Antibodies
MAGT1 (Magnesium Transporter 1 (MAGT1))

Reactivity

  • 16
  • 11
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human, Mouse

Host

  • 16
Rabbit

Clonality

  • 16
Polyclonal

Conjugate

  • 10
  • 2
  • 1
  • 1
  • 1
  • 1
This MAGT1 antibody is un-conjugated

Application

  • 16
  • 11
  • 10
  • 2
  • 1
  • 1
Western Blotting (WB), Flow Cytometry (FACS)
  • Binding Specificity

    • 8
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 44-71, N-Term

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This MAGT1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 44-71 amino acids from the N-terminal region of human MAGT1.

    Isotype

    Ig Fraction
  • Application Notes

    For WB starting dilution is: 1:1000

    For FACS starting dilution is: 1:10~50

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5 mg/mL

    Buffer

    Supplied in PBS with 0.09 % (W/V) 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 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
  • Target

    MAGT1 (Magnesium Transporter 1 (MAGT1))

    Alternative Name

    MAGT1

    Background

    MAGT1 encodes a magnesium cation transporter protein that localizes to the cell membrane. This protein also associates with N-oligosaccharyl transferase and therefore may have a role in N-glycosylation. Mutations in this gene cause mental retardation X-linked type 95 (MRX95). This gene may have multiple in-frame translation initiation sites, one of which would encode a shorter protein with an N-terminus containing a signal peptide at amino acids 1-29.

    Molecular Weight

    38 kDa

    Gene ID

    84061

    UniProt

    Q9H0U3

    Pathways

    Cell RedoxHomeostasis
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