DYNAP Antikörper (N-Term)

Produktnummer ABIN950798

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

Kurzübersicht für DYNAP Antikörper (N-Term) (ABIN950798)

Target: DYNAP (Dynactin Associated Protein (DYNAP))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser DYNAP Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Enzyme Immunoassay (EIA)

Produktdetails anti-DYNAP Antikörper

Bindungsspezifität: AA 5-34, N-Term

Spezifität: This antibody reacts to C18orf26.

Kreuzreaktivität (Details): Species reactivity (tested):Human.

Aufreinigung: Affinity chromatography on Protein A

Immunogen: KLH conjugated synthetic peptide between 5-34 amino acids from the N-terminal region of human C18orf26

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 the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Details zu DYNAP

Target: DYNAP (Dynactin Associated Protein (DYNAP))

Andere Bezeichnung: C18orf26

Hintergrund: C18orf26 (chromosome 18 open reading frame 26) is a 210 amino acid single pass membrane protein that is encoded by a gene which maps to human chromosome 18. Chromosome 18 houses over 300 protein-coding genes and contains nearly 76 million nucleotide bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.Synonyms: Uncharacterized protein

Gen-ID: 284254

NCBI Accession: NP_775900