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Nyctalopin antibody (N-Term)

The Rabbit Polyclonal anti-Nyctalopin antibody has been validated for WB and EIA. It is suitable to detect Nyctalopin in samples from Human.
Catalog No. ABIN953798

Quick Overview for Nyctalopin antibody (N-Term) (ABIN953798)

Target

See all Nyctalopin (NYX) Antibodies
Nyctalopin (NYX)

Reactivity

  • 11
  • 1
Human

Host

  • 11
Rabbit

Clonality

  • 11
Polyclonal

Conjugate

  • 6
  • 1
  • 1
  • 1
  • 1
  • 1
This Nyctalopin antibody is un-conjugated

Application

  • 11
  • 9
  • 2
Western Blotting (WB), Enzyme Immunoassay (EIA)
  • Binding Specificity

    • 8
    • 2
    • 2
    • 1
    AA 59-89, N-Term

    Specificity

    This antibody recognizes Human Nyctalopin (N-term).

    Purification

    Protein A column, followed by peptide affinity purification

    Immunogen

    KLH conjugated synthetic peptide between 59~89 amino acids from the N-terminal region of Human Nyctalopin. Genename: NYX

    Isotype

    Ig Fraction
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.25 mg/mL

    Buffer

    PBS containing 0.09 % (W/V) Sodium Azide as preservative

    Preservative

    Sodium azide

    Precaution of Use

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

    Handling Advice

    Avoid repeated freezing and thawing.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Target

    Nyctalopin (NYX)

    Alternative Name

    Nyctalopin

    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].Synonyms: CLRP, NYX

    Molecular Weight

    52000 Da

    Gene ID

    60506

    NCBI Accession

    NP_072089
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