5-Methyltetrahydrofolate-Homocysteine Methyltransferase (MTR) Peptid
MTR
Reaktivität: Human
Wirt: Synthetic
BP, WB
Produktnummer ABIN980359
Kurzübersicht für 5-Methyltetrahydrofolate-Homocysteine Methyltransferase (MTR) Peptid (ABIN980359)
Target
MTR
(5-Methyltetrahydrofolate-Homocysteine Methyltransferase (MTR))
Spezies
Human
Quelle
Synthetic
Applikation
Blocking Peptide (BP), Western Blotting (WB)
-
-
Produktmerkmale
- This is a synthetic peptide designed for use in combination with anti-MTR antibody (Catalog #: ARP48473_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.
-
Aufreinigung
- Purified
-
-
5-Methyltetrahydrofolate-Homocysteine Methyltransferase (MTR) peptide
MTR Reaktivität: Human, Hund, Maus, Schwein, Ratte Wirt: Synthetic BP, Imm
-
-
Applikationshinweise
- Each Investigator should determine their own optimal working dilution for specific applications.
-
Beschränkungen
- Nur für Forschungszwecke einsetzbar
-
-
-
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.
-
-
- MTR (5-Methyltetrahydrofolate-Homocysteine Methyltransferase (MTR))
-
Hintergrund
-
MTR is the enzyme 5-methyltetrahydrofolate-homocysteine methyltransferase. This enzyme, also known as cobalamin-dependent methionine synthase, catalyzes the final step in methionine biosynthesis. Mutations in MTR have been identified as the underlying cause of methylcobalamin deficiency complementation group G. MTR encodes the enzyme 5-methyltetrahydrofolate-homocysteine methyltransferase. This enzyme, also known as cobalamin-dependent methionine synthase, catalyzes the final step in methionine biosynthesis. Mutations in MTR have been identified as the underlying cause of methylcobalamin deficiency complementation group G. Sequence Note: This RefSeq record was created from transcript and genomic sequence data because no single transcript was available for the full length of the gene. The extent of this transcript is supported by transcript alignments. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Alias Symbols: FLJ45386, MS, cblG
Protein Interaction Partner: DYNLL1,TSC22D1
Protein Size: 1265 -
Molekulargewicht
- 140 kDa
-
Gen-ID
- 4548
-
NCBI Accession
- NM_000254, NP_000245
-
UniProt
- Q99707
Target
-
Sie sind hier:
