PROKR2 polyclonal antibody
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More Files
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Western Blot (Tissue lysate)
PROKR2 polyclonal antibody (Cat # PAB17272) (1 ug/mL) staining of rat stomach lysate (35 ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.
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Specification
Product Description
Goat polyclonal antibody raised against synthetic peptide of PROKR2.
Immunogen
A synthetic peptide corresponding to amino acids at internal region of human PROKR2.
Sequence
C-NGNTSFTPNFN
Host
Goat
Theoretical MW (kDa)
44
Reactivity
Human, Rat
Form
Liquid
Purification
Antigen affinity purification
Concentration
0.5 mg/mL
Recommend Usage
ELISA (1:32000)
Western Blot (0.3-1 ug/mL)
The optimal working dilution should be determined by the end user.Storage Buffer
In Tris saline, pH 7.3 (0.5% BSA, 0.02% sodium azide)
Storage Instruction
Store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Western Blot (Tissue lysate)
PROKR2 polyclonal antibody (Cat # PAB17272) (1 ug/mL) staining of rat stomach lysate (35 ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.Enzyme-linked Immunoabsorbent Assay
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Gene Info — PROKR2
Entrez GeneID
128674Protein Accession#
NP_658986.1Gene Name
PROKR2
Gene Alias
GPR73L1, GPR73b, GPRg2, KAL3, PKR2, dJ680N4.3
Gene Description
prokineticin receptor 2
Gene Ontology
HyperlinkGene Summary
Prokineticins are secreted proteins that can promote angiogenesis and induce strong gastrointestinal smooth muscle contraction. The protein encoded by this gene is an integral membrane protein and G protein-coupled receptor for prokineticins. The encoded protein is similar in sequence to GPR73, another G protein-coupled receptor for prokineticins. [provided by RefSeq
Other Designations
G protein-coupled receptor 73-like 1|OTTHUMP00000030192
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Interactome
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Disease
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Publication Reference
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PROKR2 missense mutations associated with Kallmann syndrome impair receptor signalling activity.
Monnier C, Dode C, Fabre L, Teixeira L, Labesse G, Pin JP, Hardelin JP, Rondard P.
Human Molecular Genetics 2008 Sep; 18(1):75.
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PROKR2 missense mutations associated with Kallmann syndrome impair receptor signalling activity.
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