Mitochondrial Ribosomal Protein L49 (MRPL49) (N-Term) Peptid
MRPL49
Reaktivität: Human
Wirt: Synthetic
BP, WB
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- Target Alle MRPL49 Produkte
- MRPL49 (Mitochondrial Ribosomal Protein L49 (MRPL49))
- Protein Region
- N-Term
- Spezies
- Human
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Quelle
- Synthetic
- Applikation
- Blocking Peptide (BP), Western Blotting (WB)
- Sequenz
- IMVTFRNQAS RPYSFYSSLI SYEEDQRQGA EPRKNFVKPN ETKTYFWKVQ
- Produktmerkmale
- This is a synthetic peptide designed for use in combination with anti-MRPL49 Antibody. 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.
- Aufreinigung
- Purified
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- Applikationshinweise
- Each Investigator should determine their own optimal working dilution for specific applications.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Lyophilized
- Rekonstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Konzentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Handhabung
- Avoid repeated freeze-thaw cycles.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Target
- MRPL49 (Mitochondrial Ribosomal Protein L49 (MRPL49))
- Hintergrund
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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.
Alias Symbols: C11orf4, L49mt, MGC10656, NOF, NOF1, MRP-L49
Protein Interaction Partner: ASGR2,CALR,CANX,F10,F2,F9,HSPA5,LMAN1,LRP1,MCFD2,PHYH,PROC,PROS1,VWF,CANX,F10,LMAN1,LRP1,PHYH,PROS1,VWF
Protein Size: 2351 - Molekulargewicht
- 79 kDa
- Gen-ID
- 740
- NCBI Accession
- NM_004927, NP_004918
- UniProt
- Q13405
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