Elisa 96 well

Volume : 96 Test
Species : Bovine
Uniprot ID : O77656
Short name : MMP13
Alias : MMP-13|Matrix Metalloproteinase 13|MMP-13|CLG3|MANDP1|Collagenase 3
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 : Stem Cells, Cardiovasc µLar, Metabolism

Volume : 96-test Kit. Other Volumes are also available. Please contact us.
Assay Type : Sandwich
Detection Range : 0.312-20ng/mL
Sensitivity : 0.081ng/mL
Species : Bovine
GeneName : MMP13
Alternative Names : Matrix metalloproteinase-13,MMP-13
Uniport : O77656

Volume : 96-test Kit. Other Volumes are also available. Please contact us.
Assay Type : Sandwich
Detection Range : 0.156-10ng/mL
Sensitivity : 0.068ng/mL
Species : Bovine
GeneName : MMP1
Alternative Names : Fibroblast collagenase,Matrix metalloproteinase-1MMP-1CLG
Uniport : P28053

Volume : 96 Test
Species : Bovine
Uniprot ID : P52176
Short name : MMP-9
Alias : MMP-9|Matrix Metalloproteinase 9|CLG4B|Gelatinase B|GELB|CLG4B|macrophage gelatinase|MANDP2|MMP-9|type V collagenase
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 : Cancer, Cardiovasc µLar, Metabolism

Volume : 96-test Kit. Other Volumes are also available. Please contact us.
Assay Type :
Detection Range :
Sensitivity :
Species : Bovine
GeneName : MLN
Alternative Names :
Uniport : O62820

Species Reactivity : Bovine (Bos taurus; Cattle)
UniProt : Q2KIP7
Abbreviation : MAD2L2
Alternative Names : RP3-330O12.4; MAD2B; REV7; MAD2 (mitotic arrest deficient; yeast; homolog)-like 2|MAD2 homolog|OTTHUMP00000002273|mitotic arrest deficient homolog-like 2
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?6.6%
Inter-AssayCV : ?9.8%
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 MAD2L2 in samples. An antibody specific for MAD2L2 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyMAD2L2 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for MAD2L2 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 MAD2L2 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : MAD2L2 is a component of the mitotic spindle assembly checkpoint that prevents the onset of anaphase until all chromosomes are properly aligned at the metaphase plate. MAD2L2 is a homolog of MAD2L1. The predicted 211-amino acid MAD2B protein shares 24% and 26% sequence identity with yeast Mad2 and human MAD2L1 respectively, in the conserved regions. RT-PCR analysis revealed that both human MAD2 homologs were expressed at similar high levels in a panel of cell lines. Further binding analyses determined that the interaction of MAD2L2 with ADAM9 is mediated thro µgh a proline-rich SH3-ligand domain of ADAM9. Northern blot analysis detected 1.35-kb MAD2L5 transcripts in all tissues tested, with highest expression in testis.
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 : Q3SZ71
Abbreviation : PMPCB
Alternative Names : Beta-MPP; MPP11; MPPB; MPPP52; mitochondrial processing peptidase beta subunit
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?5.3%
Inter-AssayCV : ?9.7%
Recovery : 1.05
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 PMPCB in samples. An antibody specific for PMPCB has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPMPCB present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PMPCB 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 PMPCB bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : PMPCb is a member of the peptidase M16 family and encodes a protein with a zinc-binding motif. This protein is located in the mitochondrial matrix and catalyzes the cleavage of the leader peptides of precursor proteins newly imported into the mitochondria, tho µgh it only functions as part of a heterodimeric complex.In in vitro assays, MPPB bound frataxin, which was cleaved by the reconstituted MPP heterodimer. MPP cleavage of frataxin res µLted in an intermediate form, comprising amino acids 41 to 210, which was processed further to the mature form. In vitro and in vivo experiments s µggested that 2 C-terminal missense mutations found in FRDA patients, I151F and G130V, mod µLated interaction with MPP-beta, res µLting in a slower maturation process at the normal cleavage site.
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 : Q0P5M8
Abbreviation : PMPCA
Alternative Names : RP11-413M3.1; Alpha-MPP; FLJ26258; INPP5E; KIAA0123; MGC104197; inositol polyphosphate-5-phosphatase; 72 kD|mitochondrial matrix processing protease; alpha subunit
Application : ELISA
Range : 0.156-10 ng/mL
Sensitivity : 0.055 ng/mL
Intra-AssayCV : ?4.6%
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 PMPCA in samples. An antibody specific for PMPCA has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPMPCA present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PMPCA 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 PMPCA bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : By sequencing clones obtained from a Volume-fractionated KG-1 myeloid leukemia cell line cDNA library, Nagase et al. (1995) cloned PMPCA, which they designated KIAA0123. The deduced 528-amino acid protein contains an ins µLinase (IDE) motif and shares 85.5% identity with the rat mitochondrial processing protease. Northern blot analysis detected PMPCA expression in all tissues and cell lines examined, with highest expression in HeLa cells, heart, skeletal muscle, and testis. Hartz (2009) mapped the PMPCA gene to chromosome 9q34.3 based on an alignment of the PMPCA sequence with the genomic sequence (GRCh37). The PMPCA gene overlaps the INPP5E gene and is transcribed in the opposite direction.
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 : P54149
Abbreviation : MSRA
Alternative Names : Cytosolic methionine-S-s µLfoxide reductase|peptide met (O) reductase
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?5.3%
Inter-AssayCV : ?7.9%
Recovery : 0.95
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 MSRA in samples. An antibody specific for MSRA has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyMSRA present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for MSRA 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 MSRA 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 : Q56JY4
Abbreviation : TOMM6
Alternative Names : DKFZp761H221; FLJ32622; OBTP; over-expressed breast tumor protein|translocase of outer mitochondrial membrane 6 homolog
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?6.2%
Inter-AssayCV : ?9.2%
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 TOMM6 in samples. An antibody specific for TOMM6 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyTOMM6 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for TOMM6 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 TOMM6 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : C6ORF49 is a member of the LIM domain protein family. C6ORF49 gene contains 9 exons and spans 8.585 kb. By database searching with human PRICKLE1 and PRICKLE2 as probes, Teufel et al. (2005) identified C6ORF49, which they called OEBT, and used this sequence to identify the mouse and rat homologs. The deduced 385-amino acid C6ORF49 protein shares 72% and 54% sequence identity with the mouse and rat homologs, respectively. C6ORF49 contains 2 LIM domains and a PET domain. It is predicted to be localized in the nucleus. EST database analysis revealed C6ORF49 expression in a broad range of normal tissues as well as in hepatocell µLar carcinoma, breast cancer, and prostate cancer tissues.
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 : A8YXZ8
Abbreviation : TOMM5
Alternative Names : RP11-613M10.3; C9orf105; RP11-263I4.1; Tom5; bA613M10.3; mitochondrial outer membrane protein TOM5|translocase of outer mitochondrial membrane 5 homolog
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?6.3%
Inter-AssayCV : ?8.9%
Recovery : 1
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 TOMM5 in samples. An antibody specific for TOMM5 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyTOMM5 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for TOMM5 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 TOMM5 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : The fungal preprotein translocase of the mitochondrial outer membrane (TOM complex) comprises import receptors Tom70, Tom20, and Tom22, import channel Tom40, and small Tom proteins Tom5, Tom6, and Tom7, which reg µLate TOM complex assembly. These components are conserved in mammals; unlike the other components, however, Tom5 and Tom6 remain unidentified in mammals. These small Tom proteins are associated with Tom40 in the TOM complex. Knockdown of Tom7, but not Tom5 and Tom6, strongly compromised stability of the TOM complex. Conversely, knockdown of hTom40 decreased the level of all small Tom proteins. Matrix import of preprotein was affected by double knockdown of any combination of small Tom proteins. These res µLts indicate that human small Tom proteins maintain the structural integrity of the TOM complex.
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).