PDE11 rabbit pAb

PDE11 rabbit pAb

AO-06-ES14188-100

PDE11 rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES14188
Product namePDE11 rabbit pAb
ReactivityHuman; Mouse;Rat
ApplicationsWB;ELISA;IHC
Other name
Size100μL
Unit price ($)248
Human gene ID50940
Human Swiss-ProtQ9HCR9
SourceRabbit
IsotypeIgG
TargetPDE11
Fields>>Purine metabolism;>>Metabolic pathways;>>Cushing syndrome;>>Morphine addiction
Gene namePDE11A
Protein namePDE11
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID241489
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtP0C1Q2
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID140928
Rat gene linkView Rat Gene
Rat Swiss-ProtQ8VID6
Rat Swiss linkView Rat Swiss-Prot
ImmunogenSynthesized peptide derived from human PDE11 AA range: 421-471
SpecificityThis antibody detects endogenous levels of PDE11 at Human/Mouse/Rat
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWB 1:500-2000;IHC-p 1:50-300; ELISA 2000-20000
PurificationThe antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)103kD
Observed band (KD)
BackgroundThe 3',5'-cyclic nucleotides cAMP and cGMP function as second messengers in a wide variety of signal transduction pathways. 3',5'-cyclic nucleotide phosphodiesterases (PDEs) catalyze the hydrolysis of cAMP and cGMP to the corresponding 5'-monophosphates and provide a mechanism to downregulate cAMP and cGMP signaling. This gene encodes a member of the PDE protein superfamily. Mutations in this gene are a cause of Cushing disease and adrenocortical hyperplasia. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008],
Functioncatalytic activity:Adenosine 3',5'-cyclic phosphate + H(2)O = adenosine 5'-phosphate.,catalytic activity:Guanosine 3',5'-cyclic phosphate + H(2)O = guanosine 5'-phosphate.,cofactor:Divalent cations.,disease:Defects in PDE11A are the cause of primary pigmented nodular adrenocortical disease type 2 (PPNAD2) [MIM:610475]. Primary pigmented nodular adrenocortical disease is a rare bilateral adrenal defect causing ACTH-independent Cushing syndrome. PPNAD2 is characterized by adrenal glands with overall normal size and weight, and multiple small yellow-to-dark brown nodules surrounded by a cortex with a uniform appearance. Microscopically, there are moderate diffuse cortical hyperplasia with mostly nonpigmented nodules, multiple capsular deficits and massive circumscribed and infiltrating extra-adrenal cortical excrescences with micronodules. PPNAD2 leads to Cushing syndrome.,domain:The tandem
Subcellular locationCytoplasm, cytosol .
ExpressionIsoform 1 is present in prostate, pituitary, heart and liver. It is however not present in testis nor in penis, suggesting that weak inhibition by Tadalafil (Cialis) is not relevant (at protein level). Isoform 2 may be expressed in testis. Isoform 4 is expressed in adrenal cortex.

Additional Images

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Western blot analysis of lysates from HCT116 cells, primary antibody was diluted at 1:1000, 4°over night
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Immunohistochemical analysis of paraffin-embedded human uterus. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).
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: AO-06-ES14188-100
: 10 Items
Hurry! only 10 items left in stock.

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