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

Ceramide Kinase-Like (CERKL) Peptid

CERKL Reaktivität: Säugetier Wirt: Synthetic BP, WB, IHC
Produktnummer ABIN936925
  • Target Alle CERKL Produkte
    CERKL (Ceramide Kinase-Like (CERKL))
    Protein-Typ
    Synthetic
    Spezies
    Säugetier
    Quelle
    • 4
    Synthetic
    Applikation
    Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
    Sequenz
    ASVKNQFNFP FVETYTVEEV KVHPRNNTGG YNPEEEEDET ASENCFPWNV
    Produktmerkmale
    A synthetic peptide for use as a blocking control in assays to test for specificity of CERKL antibody,
    Alternative Names: CERKL control peptide, CERKL antibody Blocking Peptide, Anti-CERKL Blocking Peptide, ceramide kinase-like Blocking Peptide, RP26 Blocking Peptide
  • Applikationshinweise
    Optimal conditions should be determined by the investigator
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Rekonstitution
    Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
    Buffer
    PBS
    Handhabung
    Avoid repeated freeze/thaw cycles.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20 °C long term.
  • Target
    CERKL (Ceramide Kinase-Like (CERKL))
    Synonyme
    RGD1561057 Peptide, Gm1958 Peptide, Rp26 Peptide, GB19002 Peptide, RP26 Peptide, zgc:162213 Peptide, ceramide kinase like Peptide, ceramide kinase-like Peptide, ceramide kinase Peptide, CERKL Peptide, Cerkl Peptide, LOC408315 Peptide, CERK Peptide, LOC100566923 Peptide, LOC100645684 Peptide, cerkl Peptide
    Hintergrund
    This gene was initially identified as a locus (RP26) associated with an autosomal recessive form of retinitis pigmentosa (arRP) disease. This gene encodes a protein with ceramide kinase-like domains, however, the protein does not phosphorylate ceramide and its target substrate is currently unknown. This protein may be a negative regulator of apoptosis in photoreceptor cells. Mutations in this gene cause a form of retinitis pigmentosa characterized by autosomal recessive cone and rod dystrophy (arCRD). Alternative splicing of this gene results in multiple transcript variants encoding different isoforms and non-coding transcripts.
    Molekulargewicht
    51 kDa
Sie sind hier:
Kundenservice