Anti-Prokineticin 2/PK2 antibody (ab76747)
- Datasheet
- References (1)
- Protocols
Overview
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Product name
Anti-Prokineticin 2/PK2 antibody
See all Prokineticin 2/PK2 primary antibodies -
Description
Rabbit polyclonal to Prokineticin 2/PK2 -
Host species
Rabbit -
Tested applications
Suitable for: WB, IHC-Fr, IHC-Pmore details -
Species reactivity
Reacts with: Mouse, Rat, Human -
Immunogen
Synthetic peptide corresponding to Human Prokineticin 2/PK2 (C terminal).
(Peptide available asab140536) -
General notes
This product was previously labelled as Prokineticin 2
Properties
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Form
Liquid -
Storage instructions
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid repeated freeze / thaw cycles. -
Storage buffer
Constituent: Whole serum -
Purity
Whole antiserum -
Clonality
Polyclonal -
Isotype
IgG -
Research areas
Associated products
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Compatible Secondaries
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Isotype control
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Recombinant Protein
Applications
Our Abpromise guarantee covers the use of ab76747 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Application | Abreviews | Notes |
---|---|---|
WB | 1/200. Predicted molecular weight: 14 kDa. | |
IHC-Fr | 1/100 - 1/1000. | |
IHC-P | 1/100 - 1/1000. |
Target
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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. -
Tissue specificity
Expressed in the testis and, at low levels, in the small intestine. -
Involvement in disease
Defects in PROK2 are the cause of Kallmann syndrome type 4 (KAL4) [MIM:610628]; also known as hypogonadotropic hypogonadism and anosmia. 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. KAL4 patients have variable degrees of olfactory and reproductive dysfunction, but do not show any of the occasional clinical anomalies reported in Kallmann syndrome such as renal agenesis, cleft lip/palate, selective tooth agenesis, and bimanual synkinesis. -
Sequence similarities
Belongs to the AVIT (prokineticin) family. -
Cellular localization
Secreted. - Information by UniProt
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Database links
- Entrez Gene: 60675 Human
- Entrez Gene: 50501 Mouse
- Entrez Gene: 192206 Rat
- Omim: 607002 Human
- SwissProt: Q9HC23 Human
- SwissProt: Q9QXU7 Mouse
- SwissProt: Q8R413 Rat
- Unigene: 528665 Human
see all -
Alternative names
- BV8 antibody
- Bv8 homolog antibody
- MIT1 antibody
see all
Images
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Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Prokineticin 2/PK2 antibody (ab76747)
A: ab76747 staining Prokinectin 2 in Mouse testis by Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections).
B: Negative control treated with preimmune serum.
Both sections counterstained with haematoxylin.
Datasheets and documents
References
This product has been referenced in:
- Mundim MV et al. A new function for Prokineticin 2: Recruitment of SVZ-derived neuroblasts to the injured cortex in a mouse model of traumatic brain injury. Mol Cell Neurosci 94:1-10 (2019). Read more (PubMed: 30391355) »