Telefon:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@antikoerper-online.de

NSUN5P2 Antikörper

Der Kaninchen Polyklonal Anti-NSUN5P2-Antikörper wurde für WB und ELISA validiert. Er ist geeignet, NSUN5P2 in Proben von Human zu detektieren.
Produktnummer ABIN2463242

Kurzübersicht für NSUN5P2 Antikörper (ABIN2463242)

Target

NSUN5P2 (NOP2/Sun Domain Family, Member 5 Pseudogene 2 (NSUN5P2))

Reaktivität

  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Wirt

  • 3
Kaninchen

Klonalität

  • 3
Polyklonal

Konjugat

  • 3
Dieser NSUN5P2 Antikörper ist unkonjugiert

Applikation

  • 3
  • 1
  • 1
Western Blotting (WB), ELISA
  • Aufreinigung

    Antibody is purified by protein A chromatography method.

    Immunogen

    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human NSUN5C.
  • Applikationshinweise

    NSUN5C antibody can be used for detection of NSUN5C by ELISA at 1:312500. NSUN5C antibody can be used for detection of NSUN5C by western blot at 2.5 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Add 100 ?L of distilled water. Final antibody concentration is 1 mg/mL.

    Konzentration

    1 mg/mL

    Buffer

    Antibody is lyophilized in PBS buffer with 2 % sucrose.

    Handhabung

    As with any antibody avoid repeat freeze-thaw cycles.

    Lagerung

    4 °C/-20 °C

    Informationen zur Lagerung

    For short periods of storage (days) store at 4 °C. For longer periods of storage, store NSUN5C antibody at -20 °C.
  • Target

    NSUN5P2 (NOP2/Sun Domain Family, Member 5 Pseudogene 2 (NSUN5P2))

    Andere Bezeichnung

    NSUN5C

    Hintergrund

    NSUN5C gene shares high sequence similarity with several genes in the Williams Beuren Syndrome critical region and its deletion is associated with this disorder.This gene shares high sequence similarity with several genes in the Williams Beuren Syndrome critical region and its deletion is associated with this disorder. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.

    Molekulargewicht

    34 kDa

    Gen-ID

    260294

    NCBI Accession

    NP_115534

    UniProt

    Q63ZY6
Sie sind hier:
Chat with us!