5-Methyltetrahydrofolate-Homocysteine Methyltransferase (MTR) Peptide
MTR
Reactivité: Humain
Hôte: Synthetic
BP, WB
N° du produit ABIN980359
Aperçu rapide pour 5-Methyltetrahydrofolate-Homocysteine Methyltransferase (MTR) Peptide (ABIN980359)
Antigène
MTR
(5-Methyltetrahydrofolate-Homocysteine Methyltransferase (MTR))
Origine
Humain
Source
Synthetic
Application
Blocking Peptide (BP), Western Blotting (WB)
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Attributs du produit
- 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.
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Purification
- Purified
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5-Methyltetrahydrofolate-Homocysteine Methyltransferase (MTR) peptide
MTR Reactivité: Humain, Chien, Souris, Porc, Rat Hôte: Synthetic BP, Imm
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Indications d'application
- Each Investigator should determine their own optimal working dilution for specific applications.
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
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Concentration
- 1 mg/mL
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Buffer
- Final peptide concentration is 1 mg/mL in PBS.
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Conseil sur la manipulation
- Avoid repeated freeze-thaw cycles.
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Stock
- -20 °C
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Stockage commentaire
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- MTR (5-Methyltetrahydrofolate-Homocysteine Methyltransferase (MTR))
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Sujet
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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 -
Poids moléculaire
- 140 kDa
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ID gène
- 4548
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NCBI Accession
- NM_000254, NP_000245
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UniProt
- Q99707
Antigène
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