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

MRPL49 Reactivity: Human Host: Synthetic BP, WB
Catalog No. ABIN8105551
$145.08
Plus shipping costs $50.00
100 μg
Shipping to: United States
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Quick Overview for Mitochondrial Ribosomal Protein L49 (MRPL49) (N-Term) Peptide (ABIN8105551)

Target

MRPL49 (Mitochondrial Ribosomal Protein L49 (MRPL49))

Origin

Human

Source

  • 3
Synthetic

Application

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

    N-Term

    Purpose

    MRPL49 Peptide - N-terminal region

    Sequence

    IMVTFRNQAS RPYSFYSSLI SYEEDQRQGA EPRKNFVKPN ETKTYFWKVQ
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Comment

    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.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

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

    Buffer

    Lyophilized powder

    Storage

    -20 °C

    Storage Comment

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

    MRPL49 (Mitochondrial Ribosomal Protein L49 (MRPL49))

    Background

    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

    Molecular Weight

    79kDa

    Gene ID

    740

    NCBI Accession

    NP_004918

    UniProt

    Q13405
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