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Nyctalopin antibody (AA 139-189)

This Rabbit Polyclonal antibody specifically detects Nyctalopin in WB. It exhibits reactivity toward Human and Mouse.
Catalog No. ABIN8123495
$385.00
Plus shipping costs $50.00
50 μL
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for Nyctalopin antibody (AA 139-189) (ABIN8123495)

Target

See all Nyctalopin (NYX) Antibodies
Nyctalopin (NYX)

Reactivity

Human, Mouse

Host

  • 12
Rabbit

Clonality

  • 12
Polyclonal

Conjugate

  • 7
  • 1
  • 1
  • 1
  • 1
  • 1
This Nyctalopin antibody is un-conjugated

Application

  • 12
  • 9
  • 2
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 8
    • 3
    • 2
    • 2
    AA 139-189

    Purpose

    NYX Antibody

    Specificity

    This antibody detects endogenous levels of NYX at Human/Mouse

    Purification

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

    Immunogen

    Synthesized peptide derived from human NYX AA range: 139-189

    Isotype

    IgG
  • Application Notes

    WB 1:500-2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % 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

    -20 °C

    Storage Comment

    Store at -20°C/1 year

    Expiry Date

    12 months
  • Target

    Nyctalopin (NYX)

    Alternative Name

    NYX

    Background

    Background: The product of this gene belongs to the small leucine-rich proteoglycan (SLRP) family of proteins. Defects in this gene are the cause of congenital stationary night blindness type 1 (CSNB1), also called X-linked congenital stationary night blindness (XLCSNB). CSNB1 is a rare inherited retinal disorder characterized by impaired scotopic vision, myopia, hyperopia, nystagmus and reduced visual acuity. The role of other SLRP proteins suggests that mutations in this gene disrupt developing retinal interconnections involving the ON-bipolar cells, leading to the visual losses seen in patients with complete CSNB. [provided by RefSeq, Oct 2008],

    Gene Name: NYX CLRP

    Protein Name: NYX

    Gene ID

    60506

    UniProt

    Q9GZU5
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