GLYATL1 Antikörper (AA 101-200) (Biotin)

Produktnummer ABIN1700010

Dieses Anti-GLYATL1-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von GLYATL1 in WB, ELISA, IHC (p) und IHC (fro). Geeignet für Human.

Kurzübersicht für GLYATL1 Antikörper (AA 101-200) (Biotin) (ABIN1700010)

Target: GLYATL1 (Glycine-N-Acyltransferase-Like 1 (GLYATL1))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser GLYATL1 Antikörper ist konjugiert mit Biotin

Applikation: Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Produktdetails anti-GLYATL1 Antikörper (Biotin)

Bindungsspezifität: AA 101-200

Kreuzreaktivität: Human

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human GLYATL1

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

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 for 12 months.

Haltbarkeit: 12 months

Details zu GLYATL1

Target: GLYATL1 (Glycine-N-Acyltransferase-Like 1 (GLYATL1))

Andere Bezeichnung: GLYATL1

Hintergrund:

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.