Phosphoglucomutase 1 (PGM1) (Middle Region) Peptide
PGM1
Reactivité: Humain
Hôte: Synthetic
BP, WB
N° du produit ABIN981642
Aperçu rapide pour Phosphoglucomutase 1 (PGM1) (Middle Region) Peptide (ABIN981642)
Antigène
Phosphoglucomutase 1 (PGM1)
Origine
Humain
Source
Synthetic
Application
Blocking Peptide (BP), Western Blotting (WB)
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Protein Region
- Middle Region
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Séquence
- TVEKADNFEY SDPVDGSISR NQGLRLIFTD GSRIVFRLSG TGSAGATIRL
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Attributs du produit
- This is a synthetic peptide designed for use in combination with anti-PGM1 Antibody(ARP56383_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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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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- Phosphoglucomutase 1 (PGM1)
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Sujet
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PGM1 is an isozyme of phosphoglucomutase (PGM) and belongs to the phosphohexose mutase family. There are several PGM isozymes, which are encoded by different genes and catalyze the transfer of phosphate between the 1 and 6 positions of glucose. In most cell types, this PGM isozyme is predominant, representing about 90 % of total PGM activity. In red cells, PGM2 is a major isozyme. This gene is highly polymorphic. Mutations in this gene cause glycogen storage disease type 14.
Alias Symbols: GSD14
Protein Interaction Partner: S100A1,S100B,S100A1,S100B,UBA5
Protein Size: 562 -
Poids moléculaire
- 61 kDa
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ID gène
- 5236
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NCBI Accession
- NM_002633, NP_002624
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UniProt
- P36871
Antigène
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