CERKL Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

Produktnummer ABIN2713926

Produktdetails

Target: CERKL (Ceramide Kinase-Like (CERKL))

Protein-Typ: Recombinant

Proteineigenschaft: Transcript Variant 1

Spezies: Human

Quelle: HEK-293 Cells

Aufreinigungstag / Konjugat: Dieses CERKL Protein ist gelabelt mit Myc-DYKDDDDK Tag.

Applikation: Antibody Production (AbP), Standard (STD)

Produktmerkmale:

• Recombinant human CERKL (transcript variant 1) protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Reinheit: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Anwendungsinformationen

Applikationshinweise: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Kommentare:

The tag is located at the C-terminal.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Lagerung: -80 °C

Informationen zur Lagerung: Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.

Antigendetails

Target: CERKL (Ceramide Kinase-Like (CERKL))

Andere Bezeichnung: Cerkl (CERKL Produkte)

Synonyme: RGD1561057 Protein, Gm1958 Protein, Rp26 Protein, GB19002 Protein, RP26 Protein, zgc:162213 Protein, ceramide kinase like Protein, ceramide kinase-like Protein, ceramide kinase Protein, CERKL Protein, Cerkl Protein, LOC408315 Protein, CERK Protein, LOC100566923 Protein, LOC100645684 Protein, cerkl Protein

Hintergrund: This gene was initially identified as a locus (RP26) associated with an autosomal recessive form of retinitis pigmentosa (arRP) disease. This gene encodes a protein with ceramide kinase-like domains, however, the protein does not phosphorylate ceramide and its target substrate is currently unknown. This protein may be a negative regulator of apoptosis in photoreceptor cells. Mutations in this gene cause a form of retinitis pigmentosa characterized by autosomal recessive cone and rod dystrophy (arCRD). Alternative splicing of this gene results in multiple transcript variants encoding different isoforms and non-coding transcripts.[provided by RefSeq, May 2010].

Molekulargewicht: 59.4 kDa

NCBI Accession: NP_963842