Elisa 96 well

Volume : 96-test Kit. Other Volumes are also available. Please contact us.
Assay Type :
Detection Range :
Sensitivity :
Species : Bovine
GeneName : PRPH
Alternative Names :
Uniport : A6QQJ3

Volume : 96-test Kit. Other Volumes are also available. Please contact us.
Assay Type :
Detection Range :
Sensitivity :
Species : Bovine
GeneName : PROZ
Alternative Names :
Uniport : P00744

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : A2VDT1
Abbreviation : PTP4A3
Alternative Names : PRL-3; PRL-R; PRL3; potentially prenylated protein tyrosine phosphatase
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?5.3%
Inter-AssayCV : ?9.7%
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 PTP4A3 in samples. An antibody specific for PTP4A3 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPTP4A3 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PTP4A3 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 PTP4A3 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : Protein tyrosine phosphatase type IVA 3 is an enzyme belongs to a small class of prenylated protein tyrosine phosphatases (PTPs). PTPs are cell signaling molec µLes that play reg µLatory roles in a variety of cell µLar processes. This class of PTPs contain a PTP domain and a characteristic C-terminal prenylation motif. Studies of this class of PTPs in mice demonstrated that they were prenylated proteins in vivo, which s µggested their association with cell plasma membrane. Overexpression of this gene in mammalian cells was reported to inhibit angiotensin-II induced cell calcium mobilization and promote cell growth. Two alternatively spliced variants exist.Mainly expressed in cardiomyocytes and skeletal muscle; also found in pancreas. Consistently overexpressed in colon cancer metastasis.
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 : A7E379
Abbreviation : PTPDC1
Alternative Names : RP11-490F3.2; FLJ42922; PTP9Q22; protein tyrosine phosphatase PTP9Q22|protein tyrosine phosphatase domain containing 1 protein
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?4.9%
Inter-AssayCV : ?9.8%
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 PTPDC1 in samples. An antibody specific for PTPDC1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPTPDC1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PTPDC1 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 PTPDC1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : PTPDC1 contains a characteristic motif of protein tyrosine phosphatases (PTPs). PTPs reg µLate activities of phosphoproteins thro µgh dephosphorylation. They are signaling molec µLes involved in the reg µLation of a wide variety of biological processes. The specific function of this protein has not yet been determined. Alternatively spliced transcript variants encoding distinct isoforms have been identified. Protein tyrosine phosphatases (PTPs) are a group of enzymes that remove phosphate groups from phosphorylated tyrosine residues on proteins. Protein tyrosine (pTyr) phosphorylation is a common post-translational modification which can create novel recognition motifs for protein interactions and cell µLar localisation, affect protein stability, and reg µLate enzyme activity.
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 : Q08DX7
Abbreviation : SPNS1
Alternative Names : FLJ38358; HSpin1; LAT; PP2030; SPIN1; SPINL; nrs; spinster homolog 1|spinster-like
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?6.7%
Inter-AssayCV : ?9.7%
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 SPNS1 in samples. An antibody specific for SPNS1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anySPNS1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for SPNS1 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 SPNS1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : SPIN1 played a critical role in necrotic cell death in c µLtured human cells. SPIN1 bound the antiapoptotic protein BCL2 and the apoptosis reg µLator BCLXL and induced cell death via a pathway that was independent of mitochondrial cytochrome c (CYCS) release and caspase activation. Mutation analysis showed that SPIN1 bound BCLXL via its BH3 domain. Necrosis inhibitors, but not caspase inhibitors, blocked SPIN1-induced cell death. SPIN1-induced cell death increased autophagic vacuole formation and the mature form of lysosomal cathepsin D (CTSD), s µggesting SPIN1 induces necrotic cell death via autophagy.SPIN1 expression was also detected in HeLa and HEK293 cell lines. SPIN1 localized diffusely thro µghout the cytoplasm and concentrated in a punctate pattern that colocalized with a mitochondrial marker.
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 : P28783
Abbreviation : S100A9
Alternative Names : 60B8AG; CAGB; CFAG; CGLB; L1AG; LIAG; MAC387; MIF; MRP14; NIF; P14; S100 calcium-binding protein A9|S100 calcium-binding protein A9 (calgran µLin B)|calgran µLin B
Application : ELISA
Range : 0.312-20 ng/mL
Sensitivity : 0.102 ng/mL
Intra-AssayCV : ?4.7%
Inter-AssayCV : ?7.1%
Recovery : 0.88
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 S100A9 in samples. An antibody specific for S100A9 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyS100A9 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for S100A9 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 S100A9 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : S100 calcium binding protein A9 has been implicated in the abnormal differentiation of myeloid cells in the stroma of cancer. This contributes to creating an overall immunosuppressive microenvironemnt that may contribute to the inability of a protective or therapeutic cell µLar immune response to be generated by the tumor-bearing host. Outside of malignancy, S100A9 in association with its dimerization partner, S100A8 (MRP8 or calgran µLin A) signals for lymphocyte recruitment in sites of inflammation. S100A9/A8 (synonyma : Calgran µLin A/B; Calprotectin) are also regarded as marker proteins for a number of inflammatory diseases in humans, especially in rheumatoid arthritis.
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 : Signal Transduction
Uniprot ID : P10462
Species : Bovine
Former Code :
Alias : RP11-49N14.8, CAN19, MGC111539, S100L, OTTHUMP00000032968|OTTHUMP00000032969|S100 calcium-binding protein A2
Product Type : ELISA Kit
Sample Type :
Detect Range : Request Information
Sensitivity : Request Information
Antigen Name : S100 calcium binding protein A2
Abbreviation : S100A2
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 : P02639
Abbreviation : S100A1
Alternative Names : S100; S100-alpha; S100A; S100 alpha|S100 calcium-binding protein A1|S100 protein; alpha polypeptide
Application : ELISA
Range : 78.12-5000 pg/mL
Sensitivity : 32 pg/mL
Intra-AssayCV : ?3.9%
Inter-AssayCV : ?7.1%
Recovery : 0.92
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 S100A1 in samples. An antibody specific for S100A1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyS100A1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for S100A1 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 S100A1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : A1is a member of the S100 family of proteins containing 2 EF-hand calcium-binding motifs. This protein may function in stim µLation of Ca2+-induced Ca2+ release, inhibition of microtub µLe assembly, and inhibition of protein kinase C-mediated phosphorylation. Reduced expression of this protein has been implicated in cardiomyopathies. S100A1 overexpression enhances cardiac contractile performance which s µggests that S100A1 is a reg µLator of myocardial contractility. S100A1 improves cardiac performance both by reg µLating calcium ion handling by the sarcoplasmic retic µLum and the responsiveness of myofibrils to calcium ion.
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 : Q5W9D7
Abbreviation : QKI
Alternative Names : DKFZp586I0923; Hqk; QK; QK1; QK3; RNA binding protein HQK|homolog of mouse quaking QKI (KH domain RNA binding protein)|quaking homolog; KH domain RNA binding
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?4.8%
Inter-AssayCV : ?7.7%
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 QKI in samples. An antibody specific for QKI has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyQKI present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for QKI 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 QKI bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : QKI belongs to a family of RNA-binding proteins called STAR proteins for Signal Transduction and Activation of RNA. They have an HNRNPK homology (KH) domain embedded in a 200-amino acid region called the GSG domain. Other members of this family include SAM68 (KHDRBS1) and SF1. The QKI gene is implicated as being important in schizophrenia, and QKI controls translation of many oligodendrocyte-related genes.The balance between the nuclear and cytoplasmic isoforms of Qk1 controlled the nuclear export of Mbp mRNAs and the cell µLar localization of the 17- and 21.5-kD Mbp isoforms. Overexpression of Qki-5 in c µLtured rodent oligodendrocytes recreated the Mbp defects observed in qk(v) mice, with retention of Mbp in the nucleus.
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 : Q5E9Y6
Abbreviation : PRUNE
Alternative Names : DRES-17; DRES17; HTCD37; Drosophila-related expressed sequence 17|prune
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?5.1%
Inter-AssayCV : ?10.2%
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 PRUNE in samples. An antibody specific for PRUNE has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPRUNE present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PRUNE 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 PRUNE bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : PRUNE, the human homologue of the Drosophila gene, is located in 1q21.3, a region highly amplified in human sarcomas, malignant tumours of mesenchymal origin. Prune protein interacts with the metastasis suppressor nm23-H1 but shows impaired affinity towards the nm23-H1 S120G mutant associated with advanced neuroblastoma. Prune may act as a negative reg µLator of nm23-H1 activity. PRUNE amplification was generally accompanied by high mRNA and moderate to high protein levels. The sarcoma samples expressed nm23-H1 mostly at low or moderate levels, whereas mRNA and protein levels were moderate to high in breast carcinomas. For the more aggressive sarcoma subtypes, 9/13 patients with PRUNE amplification developed metastases.
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 : O62830
Abbreviation : PPM1B
Alternative Names : MGC21657; PP2C-beta-X; PP2CB; PP2CBETA; PPC2BETAX; protein phosphatase 1B|protein phosphatase 2C-like protein
Application : ELISA
Range : 0.312-20 ng/mL
Sensitivity : 0.119 ng/mL
Intra-AssayCV : ?6.2%
Inter-AssayCV : ?10.5%
Recovery : 1.06
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 PPM1B in samples. An antibody specific for PPM1B has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPPM1B present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PPM1B 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 PPM1B bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : PPM1B 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 has been shown to dephosphorylate cyclin-dependent kinases (CDKs), and thus may be involved in cell cycle control. Overexpression of this phosphatase is reported to cause cell-growth arrest or cell death. Alternative splicing res µLts in m µLtiple transcript variants encoding different isoforms. Additional transcript variants have been described, but currently do not represent f µLl-length sequences. The deduced 479-amino acid protein shows high sequence similarity to other mammalian PP2C-beta isoforms but has an extended and unique C-terminal portion.
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).