Peroxidasin Antikörper (C-Term)

Produktnummer ABIN5517681

Dieser Kaninchen Polyklonal Antikörper detektiert spezifisch Peroxidasin in WB. Es zeigt Reaktivität gegenüber Proben von Human.

Kurzübersicht für Peroxidasin Antikörper (C-Term) (ABIN5517681)

Target: Peroxidasin (PXDN) (Peroxidasin Homolog (PXDN))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Peroxidasin Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-Peroxidasin Antikörper

Bindungsspezifität: C-Term

Verwendungszweck: PXDN Antibody - C-terminal region

Sequenz: VWQDCCEDCR TRGQFNAFSY HFRGRRSLEF SYQEDKPTKK TRPRKIPSVG

Aufreinigung: Affinity purified

Immunogen: The immunogen is a synthetic peptide directed towards the C terminal region of human PXDN

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 AAP76716-100UG

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 Peroxidasin

Target: Peroxidasin (PXDN) (Peroxidasin Homolog (PXDN))

Andere Bezeichnung: PXDN

Hintergrund:

Background Information: This gene encodes a heme-containing peroxidase that is secreted into the extracellular matrix. It is involved in extracellular matrix formation, and may function in the physiological and pathological fibrogenic response in fibrotic kidney. Mutations in this gene cause corneal opacification and other ocular anomalies, and also microphthalmia and anterior segment dysgenesis.

Gene Name: peroxidasin

Alternative Symbols: PXN, VPO, MG50, PRG2, ASGD7, COPOA, D2S448, D2S448E

Protein Name: peroxidasin homolog

Molekulargewicht: 162 kDa

Gen-ID: 7837

NCBI Accession: NP_036425

UniProt: Q92626