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VSX1 antibody (AA 125-154)

This Rabbit Polyclonal antibody specifically detects VSX1 in WB. It exhibits reactivity toward Human.
Catalog No. ABIN5538275

Quick Overview for VSX1 antibody (AA 125-154) (ABIN5538275)

Target

See all VSX1 Antibodies
VSX1 (Visual System Homeobox 1 (VSX1))

Reactivity

  • 25
  • 7
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 27
Rabbit

Clonality

  • 27
Polyclonal

Conjugate

  • 15
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This VSX1 antibody is un-conjugated

Application

  • 20
  • 10
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 7
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 125-154

    Purification

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

    Immunogen

    This VSX1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 125-154 amino acids from the Central region of human VSX1.

    Isotype

    Ig Fraction
  • Application Notes

    For WB starting dilution is: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.3 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

    VSX1 (Visual System Homeobox 1 (VSX1))

    Alternative Name

    VSX1

    Background

    VSX1 contains a paired-like homeodomain and binds to the core of the locus control region of the red/green visual pigment gene cluster. The encoded protein may regulate expression of the cone opsin genes early in development. Mutations in this gene can cause posterior polymorphous corneal dystrophy and keratoconus.

    Molecular Weight

    38 kDa

    Gene ID

    30813

    UniProt

    Q9NZR4
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