Betaine--Homocysteine S-Methyltransferase 2 (BHMT2) (Middle Region) Peptid
BHMT2
Reaktivität: Human
Wirt: Synthetic
WB, BP
Produktnummer ABIN973818
150,78 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach:
Deutschland
Lieferung in 15 bis 22 Werktagen
Kurzübersicht für Betaine--Homocysteine S-Methyltransferase 2 (BHMT2) (Middle Region) Peptid (ABIN973818)
Target
BHMT2
(Betaine--Homocysteine S-Methyltransferase 2 (BHMT2))
Spezies
Human
Quelle
Synthetic
Applikation
Western Blotting (WB), Blocking Peptide (BP)
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Protein Region
- Middle Region
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Sequenz
- GFVDLPEYPF GLESRVATRW DIQKYAREAY NLGVRYIGGC CGFEPYHIRA
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Produktmerkmale
- This is a synthetic peptide designed for use in combination with anti-BHMT2 Antibody(ARP48803_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.
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Aufreinigung
- Purified
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Applikationshinweise
- Each Investigator should determine their own optimal working dilution for specific applications.
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Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Format
- Lyophilized
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Rekonstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
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Konzentration
- 1 mg/mL
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Buffer
- Final peptide concentration is 1 mg/mL in PBS.
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Handhabung
- Avoid repeated freeze-thaw cycles.
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Lagerung
- -20 °C
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Informationen zur Lagerung
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- BHMT2 (Betaine--Homocysteine S-Methyltransferase 2 (BHMT2))
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Hintergrund
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Homocysteine is a sulfur-containing amino acid that plays a crucial role in methylation reactions. Transfer of the methyl group from betaine to homocysteine creates methionine, which donates the methyl group to methylate DNA, proteins, lipids, and other intracellular metabolites. The protein encoded by this gene is one of two methyl transferases that can catalyze the transfer of the methyl group from betaine to homocysteine. Anomalies in homocysteine metabolism have been implicated in disorders ranging from vascular disease to neural tube birth defects such as spina bifida. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
Alias Symbols: FLJ20001
Protein Size: 363 -
Molekulargewicht
- 40 kDa
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Gen-ID
- 23743
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NCBI Accession
- NM_017614, NP_060084
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UniProt
- Q9H2M3
Target
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