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Prokineticin-2 Active Protein | PROK2 active protein

Human Prokineticin-2

Gene Names
PROK2; BV8; HH4; PK2; KAL4; MIT1
Reactivity
Human
Purity
> 98% by SDS-PAGE and HPLC analysis
Synonyms
Prokineticin-2; Human Prokineticin-2; Recombinant Human ProKineticin-2; PROK2 active protein
Ordering
For Research Use Only!
Host
E Coli
Reactivity
Human
Purity/Purification
> 98% by SDS-PAGE and HPLC analysis
Form/Format
Lyophilized
Sequence
AVITGACDKD SQCGGGMCCA VSIWVKSIRI CTPMGKLGDS CHPLTR KVPF FGRRMHHTCP CLPGLACLRT SFNRFICLAQ K
Sequence Length
129
Endotoxin Level
< 0.1 ng per ug of Prokineticin-2
Biological Activity
Data not available.
Related Product Information for PROK2 active protein
Prokineticin-2 (PK2) is a cysteine-rich secreted protein that is expressed in the testis and in lower levels of the small intestine. PK2 regulates various biological functions including gastrointestinal motility, angiogenesis and circadiam rhythms. It is closely related to EG-VEGF (Prokineticin-1) and binds to two orphan B-protein-coupled receptors termed PK-R1 and PK-R2. Recombinant human Prokineticin-2 is an 8.8 kDa protein consisting of 81 amino acid residues and ten cysteine residues that potentially form five pairs of intra-molecular disulfide bonds.
Product Categories/Family for PROK2 active protein

NCBI and Uniprot Product Information

NCBI GI #
NCBI GeneID
NCBI Accession #
NCBI GenBank Nucleotide #
UniProt Accession #
Molecular Weight
8.8 kDa
NCBI Official Full Name
prokineticin-2 isoform a
NCBI Official Synonym Full Names
prokineticin 2
NCBI Official Symbol
PROK2
NCBI Official Synonym Symbols
BV8; HH4; PK2; KAL4; MIT1
NCBI Protein Information
prokineticin-2; protein Bv8 homolog
UniProt Protein Name
Prokineticin-2
Protein Family
UniProt Gene Name
PROK2
UniProt Synonym Gene Names
BV8; PK2
UniProt Entry Name
PROK2_HUMAN

NCBI Description

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. [provided by RefSeq, Jul 2008]

Uniprot Description

Function: May function as an output molecule from the suprachiasmatic nucleus (SCN) that transmits behavioral circadian rhythm. May also function locally within the SCN to synchronize output. Potently contracts gastrointestinal (GI) smooth muscle.

Subcellular location: Secreted.

Tissue specificity: Expressed in the testis and, at low levels, in the small intestine.

Induction: Activated by CLOCK and BMAL1 heterodimers and light; inhibited by period genes (PER1, PER2 and PER3) and cryptochrome genes (CRY1 and CRY2)

Probable.

Involvement in disease: Hypogonadotropic hypogonadism 4 with or without anosmia (HH4) [MIM:610628]: A disorder characterized by absent or incomplete sexual maturation by the age of 18 years, in conjunction with low levels of circulating gonadotropins and testosterone and no other abnormalities of the hypothalamic-pituitary axis. In some cases, it is associated with non-reproductive phenotypes, such as anosmia, cleft palate, and sensorineural hearing loss. Anosmia or hyposmia is related to the absence or hypoplasia of the olfactory bulbs and tracts. Hypogonadism is due to deficiency in gonadotropin-releasing hormone and probably results from a failure of embryonic migration of gonadotropin-releasing hormone-synthesizing neurons. In the presence of anosmia, idiopathic hypogonadotropic hypogonadism is referred to as Kallmann syndrome, whereas in the presence of a normal sense of smell, it has been termed normosmic idiopathic hypogonadotropic hypogonadism (nIHH).Note: The disease is caused by mutations affecting distinct genetic loci, including the gene represented in this entry. The genetics of hypogonadotropic hypogonadism involves various modes of transmission. Oligogenic inheritance has been reported in some patients carrying mutations in PROK2 as well as in other HH-associated genes including PROKR2 (Ref.8). Ref.7 Ref.8

Sequence similarities: Belongs to the AVIT (prokineticin) family.

Research Articles on PROK2

Similar Products

Product Notes

The PROK2 prok2 (Catalog #AAA691685) is an Active Protein produced from E Coli and is intended for research purposes only. The product is available for immediate purchase. The Human Prokineticin-2 reacts with Human and may cross-react with other species as described in the data sheet. The amino acid sequence is listed below: AVITGACDKD SQCGGGMCCA VSIWVKSIRI CTPMGKLGDS CHPLTR KVPF FGRRMHHTCP CLPGLACLRT SFNRFICLAQ K. It is sometimes possible for the material contained within the vial of "Prokineticin-2, Active Protein" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.

Precautions

All products in the AAA Biotech catalog are strictly for research-use only, and are absolutely not suitable for use in any sort of medical, therapeutic, prophylactic, in-vivo, or diagnostic capacity. By purchasing a product from AAA Biotech, you are explicitly certifying that said products will be properly tested and used in line with industry standard. AAA Biotech and its authorized distribution partners reserve the right to refuse to fulfill any order if we have any indication that a purchaser may be intending to use a product outside of our accepted criteria.

Disclaimer

Though we do strive to guarantee the information represented in this datasheet, AAA Biotech cannot be held responsible for any oversights or imprecisions. AAA Biotech reserves the right to adjust any aspect of this datasheet at any time and without notice. It is the responsibility of the customer to inform AAA Biotech of any product performance issues observed or experienced within 30 days of receipt of said product. To see additional details on this or any of our other policies, please see our Terms & Conditions page.

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