PROK2 Protein (Transcript Variant 2)

Catalog No. ABIN2729731

Product Details

Target: PROK2 (Prokineticin 2 (PROK2))

Protein Type: Recombinant

Protein Characteristics: Transcript Variant 2

Origin: Human

Source: Escherichia coli (E. coli)

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

Characteristics:

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

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

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

Application Details

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

Restrictions: For Research Use only

Handling

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

Handling Advice: Resuspend the protein in the desired concentration in proper buffer

Storage: -80 °C

Storage Comment: 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.

Target Details

Target: PROK2 (Prokineticin 2 (PROK2))

Alternative Name: Prok2,pk2 (PROK2 Products)

Synonyms: 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

Background: 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.

Molecular Weight: 8.8 kDa

NCBI Accession: NP_068754