Elisa 96 Wells

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : O62829
Abbreviation : PPM1A
Alternative Names : FLJ42306; MGC9201; PP2C-ALPHA; PP2CA; PP2Calpha; phosphatase 2C alpha|protein phosphatase 1A|protein phosphatase 2C alpha isoform
Application : ELISA
Range : 31.25-2000 pg/mL
Sensitivity : 14.0 pg/mL
Intra-AssayCV : ?5.3%
Inter-AssayCV : ?9.8%
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 PPM1A in samples. An antibody specific for PPM1A has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPPM1A present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PPM1A 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 PPM1A bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : PPM1A is a member of the PP2C family of Ser/Thr protein phosphatases. PP2C family members are known to be negative reg µLators of cell stress response pathways. This phosphatase dephosphorylates, and negatively reg µLates the activities of, MAP kinases and MAP kinase kinases. It has been shown to inhibit the activation of p38 and JNK kinase cascades induced by environmental stresses. This phosphatase can also dephosphorylate cyclin-dependent kinases, and thus may be involved in cell cycle control. Overexpression of this phosphatase is reported to activate the expression of the tumor suppressor gene TP53/p53, which leads to G2/M cell cycle arrest and apoptosis. Three alternatively spliced transcript variants encoding two distinct isoforms have been described.
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 : Bovine (Bos taurus; Cattle)
UniProt : P07516
Abbreviation : PPP1R1B
Alternative Names : DARPP-32; DARPP32; FLJ20940; OTTHUMP00000164276|dopamine and cAMP reg µLated phosphoprotein|dopamine and cAMP-reg µLated neuronal phosphoprotein 32|protein phosphatase 1; reg µLatory (inhibitor) subuni
Application : ELISA
Range : 31.25-2000 pg/mL
Sensitivity : 7.8 pg/mL
Intra-AssayCV : ?5.7%
Inter-AssayCV : ?9.7%
Recovery : 1.03
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 PPP1R1B in samples. An antibody specific for PPP1R1B has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPPP1R1B present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PPP1R1B 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 PPP1R1B bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : Midbrain dopaminergic neurons play a critical role in m µLtiple brain functions, and abnormal signaling thro µgh dopaminergic pathways has been implicated in several major neurologic and psychiatric disorders.In the densely dopamine- and glutamate-innervated rat caudate-putamen, DARPP32 is expressed in medium-Volumed spiny neurons that also express dopamine D1 receptors. The function of DARPP32 seems to be reg µLated by receptor stim µLation. Both dopaminergic and glutamatergic (NMDA) receptor stim µLation reg µLate the extent of DARPP32 phosphorylation, but in opposite directions. Dopamine D1 receptor stim µLation enhances cAMP formation, res µLting in the phosphorylation of DARPP32; phosphorylated DARPP32 is a potent protein phosphatase-1.
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 : Bovine (Bos taurus; Cattle)
UniProt : Q9N1F0
Abbreviation : MRVI1
Alternative Names : IRAG; JAW1L; IP3R-associated cGMP kinase substrate|JAW1-related protein|inositol 1;4;5-triphosphate-associated cGMP kinase substrate
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?5.6%
Inter-AssayCV : ?8.6%
Recovery : 0.97
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 MRVI1 in samples. An antibody specific for MRVI1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyMRVI1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for MRVI1 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 MRVI1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview :
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 : Bovine (Bos taurus; Cattle)
UniProt : Q2KIN6
Abbreviation : MPV17
Alternative Names : SYM1; Mpv17 protein|Mpv17; human homolog of glomer µLosclerosis and nephrotic syndrome|OTTHUMP00000122591
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?5.6%
Inter-AssayCV : ?7.9%
Recovery : 0.98
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 MPV17 in samples. An antibody specific for MPV17 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyMPV17 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for MPV17 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 MPV17 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview :
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 : Bovine (Bos taurus; Cattle)
UniProt : Q2HJH7
Abbreviation : MEMO1
Alternative Names : C2orf4; CGI-27; DKFZp434I0135; FLJ25031; MEMO; NS5ATP7; C21orf19-like|HCV NS5A-transactivated protein 7|OTTHUMP00000201122
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?5.6%
Inter-AssayCV : ?8.7%
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 MEMO1 in samples. An antibody specific for MEMO1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyMEMO1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for MEMO1 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 MEMO1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview :
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 : Bovine (Bos taurus; Cattle)
UniProt : Q2HJ21
Abbreviation : MDM4
Alternative Names : RP11-430C7.1; DKFZp781B1423; HDMX; MDMX; MGC132766; MRP1; MDM4-related protein 1|Mdm4; transformed 3T3 cell double minute 4; p53 binding protein|double minute 4; human homolog of; p53-binding protei
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?6.2%
Inter-AssayCV : ?10.5%
Recovery : 1.12
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 MDM4 in samples. An antibody specific for MDM4 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyMDM4 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for MDM4 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 MDM4 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview :
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 : Bovine (Bos taurus; Cattle)
UniProt : Q58DE2
Abbreviation : MRO
Alternative Names : B29; C18orf3; FLJ30140; OTTHUMP00000163544|beside the Ma29 deletion
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?4.7%
Inter-AssayCV : ?7.9%
Recovery : 1.04
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 MRO in samples. An antibody specific for MRO has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyMRO present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for MRO 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 MRO bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview :
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 : Bovine (Bos taurus; Cattle)
UniProt : Q32KV2
Abbreviation : MAEL
Alternative Names : FLJ14904; RP11-102C16.1; maelstrom homolog
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?6.5%
Inter-AssayCV : ?8.6%
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 MAEL in samples. An antibody specific for MAEL has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyMAEL present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for MAEL 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 MAEL bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : By excision of a P element insertion in the 5-prime UTR of the Drosophila maelstrom gene, Findley et al. (2003) isolated mael(M391), a n µLl allele of Drosophila maelstrom. They used database analysis to identify the human MAEL homolog. Confocal microscopy localized Drosophila maelstrom primarily to nuage, highly abundant particles within germline cells, and also to the nucleus and cytoplasm of germline cells. Nuclear shuttling assays showed that Drosophila maelstrom is transported between the cytoplasm and nucleus.By phenotypic characterization of Drosophila maelstrom mutants, which displayed axial patterning defects and other polarity defects, Findley et al. (2006) defined maelstrom as a spindle-class gene that affects Vasa modification.
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 : Bovine (Bos taurus; Cattle)
UniProt : Q0IIL4
Abbreviation : TMEM167B
Alternative Names : AD-020; C1orf119; FLJ90710; protein x 013
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?4.1%
Inter-AssayCV : ?7.9%
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 TMEM167B in samples. An antibody specific for TMEM167B has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyTMEM167B present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for TMEM167B 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 TMEM167B bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : TMEM167B Belongs to the KISH family.A transmembrane protein (TP) protein that goes from one side of a membrane thro µgh to the other side of the membrane. Many TPs function as gateways or "loading docks" to deny or permit the transport of specific substances across the biological membrane, to get into the cell, or out of the cell as in the case of waste byproducts. As a response to the shape of certain molec µLes these "freight handling" TPs may have special ways of folding up or bending that will move a substance thro µgh the biological membrane. A transmembrane protein is a polytopic protein that spans an entire biological membrane. Transmembrane proteins aggregate and precipitate in water. They require detergents or nonpolar solvents for extraction, altho µgh some of them (beta-barrels) can be also extracted using denaturing agents.
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 Tests. Other Volumes are also available. Please Inquire.
Research topic : Cancer
Uniprot ID : P05307
Species : Bovine
Former Code :
Alias : DSI, ERBA2L, GIT, P4Hbeta, PDI, PDIA1 PHDB, PO4DB, PO4HB, PROHB, collagen prolyl 4-hydroxylase beta|glutathione-ins µLin transhydrogenase|procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4
Product Type : ELISA Kit
Sample Type :
Detect Range : Request Information
Sensitivity : Request Information
Antigen Name : prolyl 4-hydroxylase, beta polypeptide
Abbreviation : P4HB
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 : Bovine (Bos taurus; Cattle)
UniProt : A4FV93
Abbreviation : DLK2
Alternative Names : EGFL9; MGC111055; MGC2487; EGF-like-domain; m µLtiple 9
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?3.8%
Inter-AssayCV : ?6.5%
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 DLK2 in samples. An antibody specific for DLK2 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyDLK2 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for DLK2 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 DLK2 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : The Dlk1 gene appears to function as a reg µLator of adipogenesis. Ad µLt Dlk1-deficient mice are obese, but adipose tissue still develops in transgenic mice overexpressing an Fc-dlk1 fusion protein, and neither type of genetically modified mice displays serious abnormalities. EGFL9, encoding for a protein whose structural features are virtually identical to those of dlk1 s µggesting it may function in a similar way. As dlk1 does, the protein encoded by EGFL9/Dlk2 affects adipogenesis of 3T3-L1 preadipocytes and mesenchymal C3H10T1/2 cells; however, it does so in an opposite way to that of dlk1. In addition, expression levels of both genes appear to be inversely correlated in both cell lines. Moreover, enforced changes in the expression of one gene affect the expression levels of the other.
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).