Elisa 96 Wells

Species Reactivity : Human (Homo sapiens)
UniProt : P31323
Abbreviation : PRKAR2B
Alternative Names : PRKAR2; RII-BETA; H_RG363E19.2|W µgSC : H_RG363E19.2|cAMP-dependent protein kinase type II-beta reg µLatory chain|cAMP-dependent protein kinase; reg µLatory subunit beta 2
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?4.7%
Inter-AssayCV : ?6.3%
Recovery : 1.01
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate PRKAR2B in samples. An antibody specific for PRKAR2B has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPRKAR2B present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PRKAR2B is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of PRKAR2B bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : The inactive holoenzyme of AMPK is a tetramer composed of two reg µLatory and two catalytic subunits. cAMP causes the dissociation of the inactive holoenzyme into a dimer of reg µLatory subunits bound to four cAMP and two free monomeric catalytic subunits. Four different reg µLatory subunits and three catalytic subunits of AMPK have been identified in humans. PRKAR2b is one of the reg µLatory subunits. This subunit can be phosphorylated by the activated catalytic subunit. This subunit has been shown to interact with and suppress the transcriptional activity of the cAMP responsive element binding protein 1 (CREB1) in activated T cells. Knockout studies in mice s µggest that this subunit may play an important role in reg µLating energy balance and adiposity.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Human (Homo sapiens)
UniProt : P13861
Abbreviation : PRKAR2A
Alternative Names : MGC3606; PKR2; PRKAR2; OTTHUMP00000210266|cAMP-dependent protein kinase reg µLatory subunit RII alpha|cAMP-dependent protein kinase; reg µLatory subunit alpha 2|protein kinase A; RII-alpha subunit
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?4.6%
Inter-AssayCV : ?8.3%
Recovery : 1.09
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate PRKAR2A in samples. An antibody specific for PRKAR2A has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPRKAR2A present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PRKAR2A is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of PRKAR2A bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : The inactive holoenzyme of PKA is a tetramer composed of two reg µLatory and two catalytic subunits. cAMP causes the dissociation of the inactive holoenzyme into a dimer of reg µLatory subunits bound to four cAMP and two free monomeric catalytic subunits. Four different reg µLatory subunits and three catalytic subunits of PKA have been identified in humans. PRKAR2a is one of the reg µLatory subunits. This subunit can be phosphorylated by the activated catalytic subunit. It may interact with various A-kinase anchoring proteins and determine the subcell µLar localization of PKA. This subunit has been shown to reg µLate protein transport from endosomes to the Golgi apparatus and further to the endoplasmic retic µLum (ER).
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Human (Homo sapiens)
UniProt : P31321
Abbreviation : PRKAR1B
Alternative Names : PRKAR1; OTTHUMP00000199948|OTTHUMP00000199949
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?4.6%
Inter-AssayCV : ?8.3%
Recovery : 0.99
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate PRKAR1B in samples. An antibody specific for PRKAR1B has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPRKAR1B present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PRKAR1B is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of PRKAR1B bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : Cyclic AMP-dependent protein kinase A (PKA) is an essential enzyme in the signaling pathway of the second messenger cAMP. Thro µgh phosphorylation of target proteins, PKA controls many biochemical events in the cell including reg µLation of metabolism, ion transport, and gene transcription. PRKAR1b is composed of 2 reg µLatory and 2 catalytic subunits and dissociates from the reg µLatory subunits upon binding of cAMP. BAD is required to assemble the complex, the lack of which res µLts in diminished mitochondria-based glucokinase activity and blunted mitochondrial respiration in response to glucose. Glucose deprivation res µLts in dephosphorylation of BAD, and BAD-dependent cell death.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Human (Homo sapiens)
UniProt : P10644
Abbreviation : PRKAR1A
Alternative Names : CAR; CNC; CNC1; DKFZp779L0468; MGC17251; PKR1; PPNAD1; PRKAR1; TSE1; cAMP-dependent protein kinase reg µLatory subunit RIalpha|cAMP-dependent protein kinase type I-alpha reg µLatory chain|cAMP-depende
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?4.2%
Inter-AssayCV : ?8.1%
Recovery : 0.96
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate PRKAR1A in samples. An antibody specific for PRKAR1A has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPRKAR1A present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PRKAR1A is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of PRKAR1A bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : cAMP is a signaling molec µLe important for a variety of cell µLar functions. cAMP exerts its effects by activating the cAMP-dependent protein kinase A (PKA), which transduces the signal thro µgh phosphorylation of different target proteins. Four different reg µLatory subunits and three catalytic subunits of PKA have been identified in humans. TSE1 is one of the reg µLatory subunits. This protein was found to be a tissue-specific extinguisher that down-reg µLates the expression of seven liver genes in hepatoma x fibroblast hybrids. Functional n µLl mutations in this gene cause Carney complex (CNC), an autosomal dominant m µLtiple neoplasia syndrome. This gene can fuse to the RET protooncogene by gene rearrangement and form the thyroid tumor-specific chimeric oncogene known as PTC2.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Human (Homo sapiens)
UniProt : P22612
Abbreviation : PRKACG
Alternative Names : KAPG; PKACg; PKA C-gamma|serine(threonine) protein kinase
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?6.4%
Inter-AssayCV : ?11.5%
Recovery : 0.99
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate PRKACG in samples. An antibody specific for PRKACG has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPRKACG present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PRKACG is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of PRKACG bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : Cyclic AMP-dependent protein kinase (PKA) consists of two catalytic subunits and a reg µLatory subunit dimer. This gene encodes the gamma form of its catalytic subunit. The gene is intronless and is tho µght to be a retrotransposon derived from the gene for the alpha form of the PKA catalytic subunit. The PRKACG gene is intronless, contains remnants of a poly(A) tail, is flanked by direct repeats, and is colinear with the PRKACA gene. Thus, the authors concluded that the PRKACG gene is a PRKACA-derived retroposon. Northern blot analysis detected PRKACG expression in fractionated germ cells of human testes.Whereas at the amino acid level C-alpha and C-beta showed 93% homology, C-gamma showed only about 80% homology to both C-alpha and C-beta.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Human (Homo sapiens)
UniProt : P22694
Abbreviation : PRKACB
Alternative Names : RP11-82H13.1; DKFZp781I2452; MGC41879; MGC9320; PKACB; PKA C-beta|cAMP-dependent protein kinase catalytic beta subunit isoform 4ab|cAMP-dependent protein kinase catalytic subunit beta|protein kinase
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?6.3%
Inter-AssayCV : ?10.9%
Recovery : 1.02
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate PRKACB in samples. An antibody specific for PRKACB has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPRKACB present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PRKACB is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of PRKACB bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : cAMP is a signaling molec µLe important for a variety of cell µLar functions. cAMP exerts its effects by activating the AMP-activated protein kinase (AMPK), which transduces the signal thro µgh phosphorylation of different target proteins. The inactive holoenzyme of AMPK is a tetramer composed of two reg µLatory and two catalytic subunits. cAMP causes the dissociation of the inactive holoenzyme into a dimer of reg µLatory subunits bound to four cAMP and two free monomeric catalytic subunits. Four different reg µLatory subunits and three catalytic subunits of AMPK have been identified in humans. PRKACB is a member of the Ser/Thr protein kinase family and is a catalytic subunit of AMPK. Three alternatively spliced transcript variants encoding distinct isoforms have been observed.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Human (Homo sapiens)
UniProt : P17612
Abbreviation : PRKACA
Alternative Names : MGC102831; MGC48865; PKACA; PKA C-alpha|cAMP-dependent protein kinase catalytic subunit alpha|cAMP-dependent protein kinase catalytic subunit alpha; isoform 1|protein kinase A catalytic subunit
Application : ELISA
Range : 0.156-10 ng/mL
Sensitivity : 0.061 ng/mL
Intra-AssayCV : ?5.8%
Inter-AssayCV : ?8.3%
Recovery : 1.09
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate PRKACA in samples. An antibody specific for PRKACA has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPRKACA present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PRKACA is added to the wells. After washing, Streptavidin conj µgated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of PRKACA bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : cAMP is a signaling molec µLe important for a variety of cell µLar functions. cAMP exerts its effects by activating the AMP-activated protein kinase (AMPK), which transduces the signal thro µgh phosphorylation of different target proteins. The inactive holoenzyme of AMPK is a tetramer composed of two reg µLatory and two catalytic subunits. cAMP causes the dissociation of the inactive holoenzyme into a dimer of reg µLatory subunits bound to four cAMP and two free monomeric catalytic subunits. Four different reg µLatory subunits and three catalytic subunits of AMPK have been identified in humans. PRKACais a member of the Ser/Thr protein kinase family and is a catalytic subunit of AMPK. Alternatively spliced transcript variants encoding distinct isoforms have been observed.
Stability : The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Volume : 96 Test
Species : Human
Uniprot ID : P49913
Short name : CAMP
Alias : CAMP|CAP 18|CAP18|CRAMP|FALL 39|FALL39|hCAP 18|HSD26|LL37
Sensitivity : 0.281ng/ml
Range : 0.469-30ng/ml
Detection method : Sandwich ELISA, Double Antibody
Storage_tempeRature : 2-8 °C for 6 months
Research Area : Immunology

Volume : 96 Tests. Other Volumes are also available. Please Inquire.
Research topic : Immunology
Uniprot ID : P16220
Species : Human
Former Code : CSB-EL005947HU
Alias : CREB, MGC9284, OTTHUMP00000206660|active transcription factor CREB|cAMP-response element-binding protein-1|transactivator protein
Product Type : ELISA Kit
Sample Type : serum, plasma, tissue homogenates
Detect Range : 0.312 ng/ml-20 ng/ml
Sensitivity : 0.078 ng/ml
Antigen Name : cAMP responsive element binding protein 1
Abbreviation : CREB1
Protein Biological Process 1 : Immunity
Protein Biological Process 2 :
Protein Biological Process 3 : Host-virus interaction
Assay Time : 1-5h
Sample Volume : 50-100 µL
Detection Wavelength : 450 nm
Delievery Date : 3-5 working days

Volume : 96 Tests. Other Volumes are also available. Please Inquire.
Research topic : Signal Transduction
Uniprot ID : Q9Y233
Species : Human
Former Code :
Alias : PDE10A，FLJ11894, FLJ25677, HSPDE10A, OTTHUMP00000017586|dJ416F21.1 (phosphodiesterase 10A)|phosphodiesterase 10A1 (PDE10A1)
Product Type : ELISA Kit
Sample Type : serum, plasma, tissue homogenates, cell lysates
Detect Range : 125 pg/ml-8000 pg/ml
Sensitivity : 31.25 pg/ml
Antigen Name : cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A (PDE10A)
Abbreviation : PDE10A
Protein Biological Process 1 :
Protein Biological Process 2 :
Protein Biological Process 3 :
Assay Time : 1-3h
Sample Volume : 50-100 µL
Detection Wavelength : 450nm
Delievery Date :

Volume : 96-test Kit. Other Volumes are also available. Please contact us.
Assay Type : Sandwich
Detection Range : 125-8000pg/mL
Sensitivity : 44pg/mL
Species : Human
GeneName : CAMP
Alternative Names : 18 kDa cationic antimicrobial protein,CAP-18,CAP18,FALL39,HSD26
Uniport : P49913