HSD17B4 Antikörper (Middle Region)

Produktnummer ABIN950184

Dieses Anti-HSD17B4-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von HSD17B4 in WB, IHC (p) und EIA. Geeignet für Human.

Kurzübersicht für HSD17B4 Antikörper (Middle Region) (ABIN950184)

Target: HSD17B4 (Hydroxysteroid (17-Beta) Dehydrogenase 4 (HSD17B4))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser HSD17B4 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)

Produktdetails anti-HSD17B4 Antikörper

Bindungsspezifität: AA 340-370, Middle Region

Spezifität: This antibody recognizes Human 17-beta-HSD4 / HSD17B4 (Center).

Aufreinigung: Protein A column, followed by peptide affinity purification

Immunogen: KLH conjugated synthetic peptide between 340-370 amino acids from the Central region of human 17-beta-HSD4 / HSD17B4

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: Optimal working dilution should be determined by the investigator.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.25 mg/mL

Buffer: PBS containing 0.09 % (W/V) Sodium Azide as preservative

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Handhabung: Avoid repeated freezing and thawing.

Lagerung: 4 °C/-20 °C

Informationen zur Lagerung: Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Details zu HSD17B4

Target: HSD17B4 (Hydroxysteroid (17-Beta) Dehydrogenase 4 (HSD17B4))

Andere Bezeichnung: 17-beta-HSD4 / HSD17B4

Hintergrund: The protein encoded by this gene is a bifunctional enzyme that is involved in the peroxisomal beta-oxidation pathway for fatty acids. It also acts as a catalyst for the formation of 3-ketoacyl-CoA intermediates from both straight-chain and 2-methyl-branched-chain fatty acids. Defects in this gene that affect the peroxisomal fatty acid beta-oxidation activity are a cause of D-bifunctional protein deficiency (DBPD). An apparent pseudogene of this gene is present on chromosome 8. [provided by RefSeq].Synonyms: 17-beta-hydroxysteroid dehydrogenase 4, D-bifunctional protein, DBP, EDH17B4, MFE-2, MFE2, Peroxisomal multifunctional enzyme type 2, SDR8C1

Molekulargewicht: 79686 Da

Gen-ID: 3295

NCBI Accession: NP_000405

Pathways: Monocarboxylic Acid Catabolic Process