Anti-human alpha

Volume : 100 µL
Host : Rabbit
Clonality : polyclonal Ab
Isotype : IgG
GeneName : HNF4A
GeneID : 3172
Uniprot : P41235
Specificity : HNF4 alpha Antibody detects endogenous levels of total HNF4 alpha.
Immunogen : A syntheVolumed peptide derived from human HNF4 alpha, corresponding to a region within the internal amino acids.
Storage : Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.Store at -20 °C.Stable for 12 months from date of receipt.
Reactivity : Human,Mouse,Rat
Prediction : Pig,Zebrafish,Bovine,Horse,Sheep,Rabbit,Dog,Chicken,Xenopus
Application : WB,IF/ICC,ELISA(peptide)
Dilution : WB 1 : 500-1 : 2000, IF/ICC 1 : 100-1 : 500, ELISA(peptide) 1 : 20000-1 : 40000
Conj µgate : Unconj µgated
RRID : AB_2835147
An Introduction to Blocking Peptides : A superior strategy for validation of antibody binding is the use of blocking peptides. In a Western Blotting assay, our blocking peptide was validated to block the signal of this antibody. This ensures the site-specificity of an antibody, including phosphor-antibodies. In the case of the phosphor- antibodies, the antibodies can and will only recognize the phosphorylated target protein at the corresponding site, not the non-phosphorylated target protein or target protein phosphorylated at a different site.
Cat# Blocking Peptide : AF6297-BP
Des# Blocking Peptide : HNF4 alpha Blocking peptide
Blocking Peptide Price : $549 CAD

Volume : 100 µL
Host : Rabbit
Clonality : polyclonal Ab
Isotype : IgG
GeneName : HNF4A,HNF4G
GeneID : 3172,3174
Uniprot : P41235/Q14541
Specificity : HNF4 alpha /gamma Antibody detects endogenous levels of total HNF4 alpha /gamma.
Immunogen : A syntheVolumed peptide derived from human HNF4 alpha /gamma, corresponding to a region within the internal amino acids.
Storage : Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.Store at -20 °C.Stable for 12 months from date of receipt.
Reactivity : Human,Mouse,Rat
Prediction : Pig,Bovine,Horse,Sheep,Rabbit,Dog
Application : WB,IF/ICC,ELISA(peptide)
Dilution : WB 1 : 500-1 : 2000, IF/ICC 1 : 100-1 : 500, ELISA(peptide) 1 : 20000-1 : 40000
Conj µgate : Unconj µgated
RRID : AB_2834237
An Introduction to Blocking Peptides : A superior strategy for validation of antibody binding is the use of blocking peptides. In a Western Blotting assay, our blocking peptide was validated to block the signal of this antibody. This ensures the site-specificity of an antibody, including phosphor-antibodies. In the case of the phosphor- antibodies, the antibodies can and will only recognize the phosphorylated target protein at the corresponding site, not the non-phosphorylated target protein or target protein phosphorylated at a different site.
Cat# Blocking Peptide : AF0534-BP
Des# Blocking Peptide : HNF4 alpha /gamma Blocking peptide
Blocking Peptide Price : $549 CAD

Volume : 100 µL
Host : Mouse
Clonality : Monoclonal
Isotype : IgG1
GeneName : HIF1A
GeneID : 3091
Uniprot : Q16665
Specificity : HIF1 alpha mouse monoclonal antibody detects endogenous levels of HIF1a.
Immunogen : A syntheVolumed peptide derived from human HIF1a.
Storage : Mouse IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.Store at -20 °C.Stable for 15 months from date of receipt.
Reactivity : Human,Mouse,Rat
Prediction :
Application : WB,IHC,IF/ICC,ELISA(peptide)
Dilution : WB 1 : 500-1 : 2000, IHC 1 : 50-1 : 200, IF/ICC 1 : 100-1 : 500
Conj µgate : Unconj µgated
RRID : AB_2846221
An Introduction to Blocking Peptides : A superior strategy for validation of antibody binding is the use of blocking peptides. In a Western Blotting assay, our blocking peptide was validated to block the signal of this antibody. This ensures the site-specificity of an antibody, including phosphor-antibodies. In the case of the phosphor- antibodies, the antibodies can and will only recognize the phosphorylated target protein at the corresponding site, not the non-phosphorylated target protein or target protein phosphorylated at a different site.
Cat# Blocking Peptide :
Des# Blocking Peptide :
Blocking Peptide Price : $549 CAD

Volume : 100 µL
Host : Rabbit
Clonality : polyclonal Ab
Isotype : IgG
GeneName : HIF3A
GeneID : 64344
Uniprot : Q9Y2N7
Specificity : HIF-3 alpha Antibody detects endogenous levels of total HIF-3 alpha.
Immunogen : A syntheVolumed peptide derived from human HIF-3 alpha, corresponding to a region within the internal amino acids.
Storage : Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.Store at -20 °C.Stable for 12 months from date of receipt.
Reactivity : Human,Mouse,Rat
Prediction : Pig,Bovine,Horse,Sheep
Application : WB,IHC,ELISA(peptide)
Dilution : WB 1 : 1000-3000, IHC 1 : 50-1 : 200, ELISA(peptide) 1 : 20000-1 : 40000
Conj µgate : Unconj µgated
RRID : AB_2841761
An Introduction to Blocking Peptides : A superior strategy for validation of antibody binding is the use of blocking peptides. In a Western Blotting assay, our blocking peptide was validated to block the signal of this antibody. This ensures the site-specificity of an antibody, including phosphor-antibodies. In the case of the phosphor- antibodies, the antibodies can and will only recognize the phosphorylated target protein at the corresponding site, not the non-phosphorylated target protein or target protein phosphorylated at a different site.
Cat# Blocking Peptide : DF8557-BP
Des# Blocking Peptide : HIF-3 alpha Blocking peptide
Blocking Peptide Price : $549 CAD

Volume : 100 µL
Host : Rabbit
Clonality : polyclonal Ab
Isotype : IgG
GeneName : EPAS1
GeneID : 2034
Uniprot : Q99814
Specificity : HIF-2-alpha Antibody detects endogenous levels of total HIF-2-alpha.
Immunogen : A syntheVolumed peptide derived from human HIF-2-alpha, corresponding to a region within the internal amino acids.
Storage : Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.Store at -20 °C.Stable for 12 months from date of receipt.
Reactivity : Human,Mouse,Rat
Prediction : Pig,Bovine,Horse,Rabbit,Dog,Xenopus
Application : WB,IF/ICC,ELISA(peptide)
Dilution : WB 1 : 1000-3000, IF/ICC, ELISA(peptide) 1 : 20000-1 : 40000
Conj µgate : Unconj µgated
RRID : AB_2840914
An Introduction to Blocking Peptides : A superior strategy for validation of antibody binding is the use of blocking peptides. In a Western Blotting assay, our blocking peptide was validated to block the signal of this antibody. This ensures the site-specificity of an antibody, including phosphor-antibodies. In the case of the phosphor- antibodies, the antibodies can and will only recognize the phosphorylated target protein at the corresponding site, not the non-phosphorylated target protein or target protein phosphorylated at a different site.
Cat# Blocking Peptide : DF2928-BP
Des# Blocking Peptide : HIF-2-alpha Blocking peptide
Blocking Peptide Price : $549 CAD

Volume : 96 Tests. Other Volumes are also available. Please Inquire.
Research topic : Cell Biology
Uniprot ID : P47710
Species : Human
Former Code :
Alias : CASA, CSN1 MGC149368, casein, alpha
Product Type : ELISA Kit
Sample Type : breast milk
Detect Range : 37.5 μg/ml-600 μg/ml
Sensitivity : 18.75 μg/ml
Antigen Name : casein alpha s1
Abbreviation : CSN1S1
Protein Biological Process 1 :
Protein Biological Process 2 :
Protein Biological Process 3 :
Assay Time : 1-5h
Sample Volume : 50-100 µL
Detection Wavelength : 450 nm
Delievery Date : 7-14 working days

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 : 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 : 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 Kit. Other Volumes are also available. Please contact us.
Assay Type : Competitive
Detection Range : 0.78-50ng/mL
Sensitivity : 0.446ng/mL
Species : Human
GeneName : CAMK2A
Alternative Names : CaM kinase II subunit alpha,CAMKA,KIAA0968
Uniport : Q9UQM7

Volume : 96 Test
Species : Human
Uniprot ID : Q9UQM7
Short name : CAMK2?
Alias : CAMK2?|CAMKA
Sensitivity : 0.094ng/ml
Range : 0.156-10ng/ml
Detection method : Sandwich ELISA, Double Antibody
Storage_tempeRature : 2-8 °C for 6 months
Research Area : Neuroscience, Signal Transduction, Cancer, Metabolism