PROK2 Protein (Transcript Variant 2)

Produktnummer ABIN2729731

Produktdetails

Target: PROK2 (Prokineticin 2 (PROK2))

Protein-Typ: Recombinant

Proteineigenschaft: Transcript Variant 2

Spezies: Human

Quelle: Escherichia coli (E. coli)

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

Produktmerkmale:

• Recombinant human PROK2 / PK2 (transcript variant 2) protein expressed in E. coli.
• Produced with end-sequenced ORF clone

Reinheit: > 95 % as determined by SDS-PAGE and Coomassie blue staining

Endotoxin-Niveau: Endotoxin level is <0.1 ng/μg of protein (<1EU/μg).

Anwendungsinformationen

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

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Buffer: Lyophilized from a 0.2 μM filtered solution of 20 mM phosphate buffer,100 mM NaCl, pH 7.2

Handhabung: Resuspend the protein in the desired concentration in proper buffer

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: PROK2 (Prokineticin 2 (PROK2))

Andere Bezeichnung: Prok2,pk2 (PROK2 Produkte)

Synonyme: PROK2 Protein, Bv8 Protein, PK2 Protein, Prok1 Protein, BV8 Protein, HH4 Protein, KAL4 Protein, MIT1 Protein, prokineticin 2 Protein, prokineticin 2 S homeolog Protein, prokineticin-2 Protein, PROK2 Protein, prok2 Protein, prok2.S Protein, Prok2 Protein, LOC101104864 Protein

Hintergrund: This gene encodes a protein expressed in the suprachiasmatic nucleus (SCN) circadian clock that may function as the output component of the circadian clock. The secreted form of the encoded protein may also serve as a chemoattractant for neuronal precursor cells in the olfactory bulb. Proteins from other vertebrates which are similar to this gene product were isolated based on homology to snake venom and secretions from frog skin, and have been shown to have diverse functions. Mutations in this gene are associated with Kallmann syndrome 4. Multiple transcript variants encoding different isoforms have been found for this gene.

Molekulargewicht: 8.8 kDa

NCBI Accession: NP_068754