GAMT anticorps (N-Term)
Aperçu rapide pour GAMT anticorps (N-Term) (ABIN2776937)
Antigène
Voir toutes GAMT AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- N-Term
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Fonction
- GAMT Antibody - N-terminal region
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Séquence
- MSAPSATPIF APGENCSPAW GAAPAAYDAA DTHLRILGKP VMERWETPYM
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Homologie
- Cow: 92%, Guinea Pig: 85%, Human: 100%, Mouse: 92%, Pig: 92%, Rat: 85%
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Attributs du produit
- This is a rabbit polyclonal antibody against GAMT. It was validated on Western Blot using a cell lysate as a positive control.
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Purification
- Affinity Purified
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Immunogène
- The immunogen is a synthetic peptide directed towards the N terminal region of human GAMT
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Indications d'application
- Optimal working dilution should be determined by the investigator.
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Commentaires
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We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP41684-100UG
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 0.5 mg/mL
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Buffer
- Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Conseil sur la manipulation
- prevent freeze-thaw cycles
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Stock
- 4 °C,-20 °C
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Stockage commentaire
- For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.
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- GAMT (Guanidinoacetate N-Methyltransferase (GAMT))
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Autre désignation
- GAMT
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Sujet
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Background Information: GAMT is a methyltransferase that converts guanidoacetate to creatine, using S-adenosylmethionine as the methyl donor. Defects in its gene have been implicated in neurologic syndromes and muscular hypotonia, probably due to creatine deficiency and accumulation of guanidinoacetate in the brain of affected individuals.The protein encoded by this gene is a methyltransferase that converts guanidoacetate to creatine, using S-adenosylmethionine as the methyl donor. Defects in this gene have been implicated in neurologic syndromes and muscular hypotonia, probably due to creatine deficiency and accumulation of guanidinoacetate in the brain of affected individuals. Two transcript variants encoding different isoforms have been described for this gene.
Gene Name: Guanidinoacetate N-methyltransferase
Alternative Symbols: PIG2, CCDS2, TP53I2, HEL-S-20
Protein Name: Guanidinoacetate N-methyltransferase
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Poids moléculaire
- 26kDa
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ID gène
- 2593
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NCBI Accession
- NP_000147
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UniProt
- Q14353
Antigène
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