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C16orf57 antibody (N-Term)

This Rabbit Polyclonal antibody specifically detects C16orf57 in WB. It exhibits reactivity toward Human.
Catalog No. ABIN5517969

Quick Overview for C16orf57 antibody (N-Term) (ABIN5517969)

Target

See all C16orf57 (USB1) Antibodies
C16orf57 (USB1) (U6 SnRNA Biogenesis 1 (USB1))

Reactivity

  • 25
  • 18
  • 18
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 22
  • 2
  • 1
Rabbit

Clonality

  • 25
Polyclonal

Conjugate

  • 8
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This C16orf57 antibody is un-conjugated

Application

  • 21
  • 13
  • 4
  • 3
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    N-Term

    Sequence

    LVGYSSSGSE DESEDGMRTR PGDGSHRRGQ SPLPRQRFPV PDSVLNMFPG

    Purification

    Affinity purified

    Immunogen

    The immunogen is a synthetic peptide directed towards the N terminal region of human C16ORF57
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

    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

    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • Target

    C16orf57 (USB1) (U6 SnRNA Biogenesis 1 (USB1))

    Alternative Name

    C16ORF57

    Background

    This gene encodes a protein with several conserved domains, however, its exact function is not known. Mutations in this gene are associated with poikiloderma with neutropenia (PN), which shows phenotypic overlap with Rothmund-Thomson syndrome (RTS) caused by mutations in the RECQL4 gene. It is believed that this gene product interacts with RECQL4 protein via SMAD4 proteins, explaining the partial clinical overlap between PN and RTS. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.

    Alias Symbols: PN, Mpn1, HVSL1, hUsb1, C16orf57

    Protein Size: 186

    Gene ID

    79650

    NCBI Accession

    NM_001195302, NP_001182231
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