GAMT Antikörper (N-Term)
Kurzübersicht für GAMT Antikörper (N-Term) (ABIN2776937)
Target
Alle GAMT Antikörper anzeigenReaktivität
Wirt
Klonalität
Konjugat
Applikation
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Bindungsspezifität
- N-Term
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Verwendungszweck
- GAMT Antibody - N-terminal region
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Sequenz
- 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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Produktmerkmale
- 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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Aufreinigung
- Affinity Purified
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Immunogen
- The immunogen is a synthetic peptide directed towards the N terminal region of human GAMT
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Applikationshinweise
- Optimal working dilution should be determined by the investigator.
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Kommentare
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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 ABIN8102022
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Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Format
- Liquid
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Konzentration
- 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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Konservierungsmittel
- Sodium azide
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Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Handhabung
- prevent freeze-thaw cycles
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Lagerung
- 4 °C,-20 °C
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Informationen zur Lagerung
- 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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Andere Bezeichnung
- GAMT
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Hintergrund
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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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Molekulargewicht
- 26kDa
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Gen-ID
- 2593
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NCBI Accession
- NP_000147
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UniProt
- Q14353
Target
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