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Acyl-CoA Synthetase Long-Chain Family Member 4 (ACSL4) (Center) Antikörper

Antigen

Acyl-CoA Synthetase Long-Chain Family Member 4 (ACSL4)

Synonyme acsl4, MGC66186, zgc:66186, ACSL4
Epitope
Alternativen

Center

Klonalität Polyklonal
Wirt
Alternativen

Kaninchen

Reaktivität
Alternativen

Human

Applikation
Alternativen Western Blot (WB), Immunhistochemie (IHC), ELISA
1 Publikation vorhanden
Zertifikate ISO 9001:2008
Produktnummer ABIN389113
Menge 0.1 mg  (0.25 mg/ml)
Preis 295,00 €   Zzgl. Versandkosten €20,00 und MWSt
Lieferung nach
Verfügbarkeit Lieferung in 7 bis 10 Werktagen

Produktbeschreibung

Produktmerkmale Purified Rabbit Polyclonal Antibody (Pab)
Weitere Bezeichnung ACSL4 (FACL4) (Center)
Gen-ID 2182
Swiss-Prot ACSL4_HUMAN
Immunogen This ACSL4 (FACL4) antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 244~274 amino acids from the center region of human FACL4.
Isotyp Ig  (Passende Sekundärantikörper)
Beschreibung Other names: Long-chain-fatty-acid--CoA ligase 4, Long-chain acyl-CoA synthetase 4, LACS4
Spezifität This antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide selected from the center region of human FACL4.
Molekulargewicht 79188 DA

Anwendungen

Applikationshinweise The suggested dilution is: ELISA~~1:1,000 Western blotting~~1:100~500 Immunohistochemistry~~1:50~100
Konzentration 0.25 mg/ml
Reinigung Purified
Buffer Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein G column, eluted with high and low pH buffers and neutralized immediately, followed by dialysis against PBS.
Lagerung Maintain refrigerated at 2-8 deg C for up to 6 months. For long term storage store at -20 deg C in small aliquots to prevent freeze-thaw cycles
Forschungsgebiet Proteinmodifikationen, Neurologie, Zellstruktur
Beschränkungen Nur für Forschungszwecke einsetzbar

Publikationen

Publikationen Rodriguez, Bhat, Meloni et al.: "Intellectual disability, midface hypoplasia, facial hypotonia, and Alport syndrome are associated with a deletion in Xq22.3." in: American journal of medical genetics. Part A, Vol. 152A, Issue 3, pp. 713-7, 2010 (PubMed).

Alternativen

Alternativen zu Antigen "Acyl-CoA Synthetase Long-Chain Family Member 4 (ACSL4)", Typ "Antikörper" finden
Wirte Ziege (1)
Reaktivitäten Rind (Kuh) (1), Hund (1), Human (1), Maus (1), Schwein (1), Ratte (Rattus) (1)
Applikationen Enzyme Immunoassay (EIA) (1), Western Blot (WB) (1)
Epitope C-Term (1)