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RNASET2 Protein (His tag)

Recombinant RNASET2-Protein exprimiert in Baculovirus infected Insect Cells.
Produktnummer ABIN7197719

Kurzübersicht für RNASET2 Protein (His tag) (ABIN7197719)

Target

Alle RNASET2 Proteine anzeigen
RNASET2 (Ribonuclease T2 (RNASET2))

Protein-Typ

Recombinant

Spezies

  • 7
  • 2
  • 2
  • 1
Human

Quelle

  • 7
  • 2
  • 1
  • 1
  • 1
Baculovirus infected Insect Cells

Reinheit

> 98 % as determined by reducing SDS-PAGE.
  • Aufreinigungstag / Konjugat

    Dieses RNASET2 Protein ist gelabelt mit His tag.

    Verwendungszweck

    Recombinant Human RNASET2 Protein (Baculovirus, His Tag)

    Sequenz

    Met 1-His 256

    Produktmerkmale

    A DNA sequence encoding the human RNASET2 isoform 1 (O00584-1) (Met 1-His 256) was fused with a polyhistidine tag at the C-terminus.

    Endotoxin-Niveau

    < 1.0 EU per μg as determined by the LAL method.
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  • Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Please refer to the printed manual for detailed information.

    Buffer

    Lyophilized from sterile 20 mM Tris, 500 mM NaCl, pH 7.4, 10 % glycerol

    Lagerung

    4 °C,-20 °C,-80 °C

    Informationen zur Lagerung

    Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80°C. Reconstituted protein solution can be stored at 4-8°C for 2-7 days. Aliquots of reconstituted samples are stable at < -20°C for 3 months.
  • Target

    RNASET2 (Ribonuclease T2 (RNASET2))

    Andere Bezeichnung

    RNASET2

    Hintergrund

    Background: RNASET2 (ribonuclease T2) is an enzyme which belongs to the RNase T2 family. It is highly expressed in the temporal lobe and fetal brain. RNASET2 gene is a novel member of the Rh/T2/S-glycoprotein class of extracellular ribonucleases. It is a single copy gene that maps to 6q27, a region associated with human malignancies and chromosomal rearrangement. Defects in RNASET2 are the cause of leukoencephalopathy cystic without megalencephaly. An infantile-onset syndrome of cerebral leukoencephalopathy. Affected newborns develop microcephaly and neurologic abnormalities including psychomotor impairment, seizures and sensorineural hearing impairment. The brain shows multifocal white matter lesions, anterior temporal lobe subcortical cysts, pericystic abnormal myelination, ventriculomegaly and intracranial calcifications.

    Synonym: Ribonuclease T2,3.1.27.-,Ribonuclease 6,RNASE6PL

    Molekulargewicht

    28.5 kDa
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