Rabbit Anti-DUSP6 Recombinant Antibody (EG1007) (CBMAB-EN1190-LY)

Basic Information
Application | Note |
ELISA | 1 µg/ml |
WB | 1:1,000-1:2,000 |
IHC-P | 1:200-1:800 |
Formulations & Storage [For reference only, actual COA shall prevail!]
Target
Plays an important role in alleviating chronic postoperative pain. Necessary for the normal dephosphorylation of the long-lasting phosphorylated forms of spinal MAPK1/3 and MAP kinase p38 induced by peripheral surgery, which drives the resolution of acute postoperative allodynia (By similarity).
Also important for dephosphorylation of MAPK1/3 in local wound tissue, which further contributes to resolution of acute pain (By similarity).
Promotes cell differentiation by regulating MAPK1/MAPK3 activity and regulating the expression of AP1 transcription factors (PubMed:29043977).
Cell differentiation Source: Ensembl
Inactivation of MAPK activity Source: UniProtKB
MAPK cascade Source: Reactome
Negative regulation of ERK1 and ERK2 cascade Source: UniProtKB
Peptidyl-threonine dephosphorylation Source: GO_Central
Peptidyl-tyrosine dephosphorylation Source: UniProtKB
Positive regulation of apoptotic process Source: UniProtKB
Protein dephosphorylation Source: GO_Central
Regulation of heart growth Source: GO_Central
Response to drug Source: Ensembl
Response to growth factor Source: Ensembl
Response to nitrosative stress Source: UniProtKB
Response to organic cyclic compound Source: Ensembl
The disease is caused by variants affecting distinct genetic loci, including the gene represented in this entry. Some patients carrying mutations in DUSP6 also have a heterozygous mutation in another HH-associated gene including FGFR1 and SPRY4 (PubMed:23643382).
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).
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Please try the standard protocols which include: protocols, troubleshooting and guide.
Enzyme-linked Immunosorbent Assay (ELISA)
Flow Cytometry
Immunofluorescence (IF)
Immunohistochemistry (IHC)
Immunoprecipitation (IP)
Western Blot (WB)
Enzyme-Linked Immunospot (ELISpot)
Proteogenomics
Other Protocols
Related Products
Rabbit Anti-DUSP6 Recombinant Antibody (CBYCD-448) (CAT#: CBMAB-D1914-YC)
Mouse Anti-DUSP6 Recombinant Antibody (3G2) (CAT#: CBMAB-D1915-YC)
Mouse Anti-DUSP6 Recombinant Antibody (CAP654) (CAT#: CBMAB-AP1959LY)
Mouse Anti-DUSP6 Recombinant Antibody (CBFYM-1079) (CAT#: V2LY-0425-LY1092)
Mouse Anti-DUSP6 Recombinant Antibody (CBYCD-449) (CAT#: CBMAB-D1916-YC)
Mouse Anti-DUSP6 Recombinant Antibody (1079) (CAT#: V2LY-0425-LY1087)
Mouse Anti-DUSP6 Recombinant Antibody (CBFYM-1078) (CAT#: V2LY-0425-LY1091)
Custom Antibody Labeling
We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).
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