EHHADH Antikörper (Middle Region)

Produktnummer ABIN5514454

Der Kaninchen Polyklonal anti-EHHADH Antikörper wird verwendet zum Nachweis von EHHADH in Proben von Human. Er wurde validiert für WB.

Kurzübersicht für EHHADH Antikörper (Middle Region) (ABIN5514454)

Target: EHHADH (Enoyl-CoA, Hydratase/3-Hydroxyacyl CoA Dehydrogenase (EHHADH))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser EHHADH Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-EHHADH Antikörper

Bindungsspezifität: Middle Region

Verwendungszweck: EHHADH Antibody - middle region

Sequenz: VIAVDSDKNQ LATANKMITS VLEKEASKMQ QSGHPWSGPK PRLTSSVKEL

Produktmerkmale: This is a rabbit polyclonal antibody against ECHP. It was validated on Western Blot.

Aufreinigung: Affinity purified

Immunogen: The immunogen is a synthetic peptide directed towards the middle region of Human ECHP

Anwendungsinformationen

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

Kommentare:

We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP76113-100UG

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.5 mg/mL

Buffer: Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

Konservierungsmittel: Sodium azide

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

Handhabung: prevent freeze-thaw cycles

Lagerung: 4 °C,-20 °C

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.

Details zu EHHADH

Target: EHHADH (Enoyl-CoA, Hydratase/3-Hydroxyacyl CoA Dehydrogenase (EHHADH))

Andere Bezeichnung: EHHADH

Hintergrund:

Background Information: The protein encoded by this gene is a bifunctional enzyme and is one of the four enzymes of the peroxisomal beta-oxidation pathway. The N-terminal region of the encoded protein contains enoyl-CoA hydratase activity while the C-terminal region contains 3-hydroxyacyl-CoA dehydrogenase activity. Defects in this gene are a cause of peroxisomal disorders such as Zellweger syndrome. Two transcript variants encoding different isoforms have been found for this gene.

Gene Name: enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase

Alternative Symbols: LBP, ECHD, LBFP, MFE1, PBFE, FRTS3, L-PBE

Protein Name: peroxisomal bifunctional enzyme

Molekulargewicht: 79kDa

Gen-ID: 1962

NCBI Accession: NP_001957

UniProt: Q08426

Pathways: Monocarboxylic Acid Catabolic Process