GLYATL1 Antikörper (AA 101-200) (AbBy Fluor® 750)
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- Target Alle GLYATL1 Antikörper anzeigen
- GLYATL1 (Glycine-N-Acyltransferase-Like 1 (GLYATL1))
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Bindungsspezifität
- AA 101-200
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser GLYATL1 Antikörper ist konjugiert mit AbBy Fluor® 750
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Applikation
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunofluorescence (Cultured Cells) (IF (cc))
- Kreuzreaktivität
- Human
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human GLYATL1
- Isotyp
- IgG
- Top Product
- Discover our top product GLYATL1 Primärantikörper
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- Applikationshinweise
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- Konservierungsmittel
- ProClin
- Vorsichtsmaßnahmen
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Haltbarkeit
- 12 months
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- Target
- GLYATL1 (Glycine-N-Acyltransferase-Like 1 (GLYATL1))
- Andere Bezeichnung
- GLYATL1 (GLYATL1 Produkte)
- Synonyme
- GATF-C antikoerper, GNAT antikoerper, glycine-N-acyltransferase like 1 antikoerper, GLYATL1 antikoerper
- Hintergrund
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Synonyms: Acyl CoA glycine N acyltransferase like protein 1, EC 2.3.1.13, FLJ26507, FLJ34646, GATF C, GATFC, Glycine N acyltransferase like 1, GNAT, MGC15397, MGC15937, GLYL1_HUMAN.
Background: GLYATL1 is a 302 amino acid mitochondrial acyltransferase that transfers the acyl group to the N-terminus of glycine. GLYATL1 can also conjugate a multitude of substrates to form a variety of N-acylglycines. A member of the glycine N-acyltransferase family, GLYATL1 exists as two alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q12.1. Chromosome 11 houses over 1,400 genes and comprises nearly 4 % of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.
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