Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

VSX2 antibody (C-Term)

This Rabbit Polyclonal antibody specifically detects VSX2 in WB. It exhibits reactivity toward Human.
Catalog No. ABIN5530826

Quick Overview for VSX2 antibody (C-Term) (ABIN5530826)

Target

See all VSX2 Antibodies
VSX2 (Visual System Homeobox 2 (VSX2))

Reactivity

  • 28
  • 13
  • 10
  • 1
Human

Host

  • 32
  • 5
  • 1
Rabbit

Clonality

  • 35
  • 3
Polyclonal

Conjugate

  • 23
  • 7
  • 4
  • 2
  • 1
  • 1
This VSX2 antibody is un-conjugated

Application

  • 38
  • 12
  • 4
  • 4
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 9
    • 8
    • 6
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 263-291, C-Term

    Purification

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

    Immunogen

    This VSX2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 263-291 amino acids from the C-terminal region of human VSX2.

    Isotype

    Ig Fraction
  • Application Notes

    For WB starting dilution is: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.41 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

    VSX2 (Visual System Homeobox 2 (VSX2))

    Alternative Name

    VSX2

    Background

    This gene encodes a homeobox protein originally described as a retina-specific transcription factor. Mutations in this gene are associated with microphthalmia, cataracts and iris abnormalities.

    Molecular Weight

    39 kDa

    Gene ID

    338917

    UniProt

    P58304

    Pathways

    Dopaminergic Neurogenesis
You are here:
Chat with us!