GATM anticorps
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- Antigène Voir toutes GATM Anticorps
- GATM (Glycine Amidinotransferase (L-Arginine:glycine Amidinotransferase) (GATM))
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Reactivité
- Humain, Souris, Rat
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp GATM est non-conjugé
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Application
- Western Blotting (WB), ELISA
- Purification
- Antibody is purified by peptide affinity chromatography method.
- Immunogène
- Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human GATM.
- Top Product
- Discover our top product GATM Anticorps primaire
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- Indications d'application
- GATM antibody can be used for detection of GATM by ELISA at 1:62500. GATM antibody can be used for detection of GATM by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
- Concentration
- 1 mg/mL
- Buffer
- Antibody is lyophilized in PBS buffer with 2 % sucrose.
- Conseil sur la manipulation
- As with any antibody avoid repeat freeze-thaw cycles.
- Stock
- 4 °C/-20 °C
- Stockage commentaire
- For short periods of storage (days) store at 4 °C. For longer periods of storage, store GATM antibody at -20 °C.
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- Antigène
- GATM (Glycine Amidinotransferase (L-Arginine:glycine Amidinotransferase) (GATM))
- Autre désignation
- GATM (GATM Produits)
- Synonymes
- anticorps AT, anticorps AGAT, anticorps CCDS3, anticorps 1810003P21Rik, anticorps AI314789, anticorps cb409, anticorps wu:fa08a06, anticorps zgc:65855, anticorps glycine amidinotransferase (L-arginine:glycine amidinotransferase) L homeolog, anticorps glycine amidinotransferase, anticorps glycine amidinotransferase (L-arginine:glycine amidinotransferase), anticorps gatm.L, anticorps GATM, anticorps Gatm, anticorps gatm
- Sujet
- GATM is a mitochondrial enzyme that belongs to the amidinotransferase family. This enzyme is involved in creatine biosynthesis, whereby it catalyzes the transfer of a guanido group from L-arginine to glycine, resulting in guanidinoacetic acid, the immediate precursor of creatine. Mutations in this gene cause arginine:glycine amidinotransferase deficiency, an inborn error of creatine synthesis characterized by mental retardation, language impairment, and behavioral disorders.This gene encodes a mitochondrial enzyme that belongs to the amidinotransferase family. This enzyme is involved in creatine biosynthesis, whereby it catalyzes the transfer of a guanido group from L-arginine to glycine, resulting in guanidinoacetic acid, the immediate precursor of creatine. Mutations in this gene cause arginine:glycine amidinotransferase deficiency, an inborn error of creatine synthesis characterized by mental retardation, language impairment, and behavioral disorders. 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.
- Poids moléculaire
- 44 kDa
- ID gène
- 2628
- NCBI Accession
- NP_001473
- UniProt
- P50440
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