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Mitochondrial Ribosomal Protein L49 (MRPL49) (N-Term) Peptid

MRPL49 Reaktivität: Human Wirt: Synthetic BP, WB
Produktnummer ABIN8105551
168,15 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach: Deutschland
Lieferung in 6 bis 9 Werktagen

Kurzübersicht für Mitochondrial Ribosomal Protein L49 (MRPL49) (N-Term) Peptid (ABIN8105551)

Target

MRPL49 (Mitochondrial Ribosomal Protein L49 (MRPL49))

Spezies

Human

Quelle

  • 3
Synthetic

Applikation

Blocking Peptide (BP), Western Blotting (WB)
  • Protein Region

    N-Term

    Verwendungszweck

    MRPL49 Peptide - N-terminal region

    Sequenz

    IMVTFRNQAS RPYSFYSSLI SYEEDQRQGA EPRKNFVKPN ETKTYFWKVQ
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Kommentare

    This is a synthetic peptide designed for use in combination with anti-MRPL49 Antibody (ARP60087_P050),. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications. Please inquire for more details.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Add 100 µL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    Buffer

    Lyophilized powder

    Lagerung

    -20 °C

    Informationen zur Lagerung

    For longer periods of storage, store at -20 °C. Avoid repeat freeze-thaw cycles.
  • Target

    MRPL49 (Mitochondrial Ribosomal Protein L49 (MRPL49))

    Hintergrund

    Background Information: This gene encodes coagulation factor VIII, which participates in the intrinsic pathway of blood coagulation, factor VIII is a cofactor for factor IXa which, in the presence of Ca+2 and phospholipids, converts factor X to the activated form Xa. This gene produces two alternatively spliced transcripts. Transcript variant 1 encodes a large glycoprotein, isoform a, which circulates in plasma and associates with von Willebrand factor in a noncovalent complex. This protein undergoes multiple cleavage events. Transcript variant 2 encodes a putative small protein, isoform b, which consists primarily of the phospholipid binding domain of factor VIIIc. This binding domain is essential for coagulant activity. Defects in this gene results in hemophilia A, a common recessive X-linked coagulation disorder.

    Alternative Symbols: C11orf4, L49mt, MGC10656, NOF, NOF1, MRP-L49

    Molekulargewicht

    79kDa

    Gen-ID

    740

    NCBI Accession

    NP_004918

    UniProt

    Q13405
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