Elisa 96 Wells

Species Reactivity : Chicken (Gallus)
UniProt : P62597
Abbreviation : POT1
Alternative Names : DKFZp586D211; HPOT1; OTTHUMP00000211676|POT1-like telomere end-binding protein|protection of telomeres 1
Application : ELISA
Range : 78-5000 pg/mL
Sensitivity : 31 pg/mL
Intra-AssayCV : ?5.1%
Inter-AssayCV : ?8.0%
Recovery : 0.94
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 POT1 in samples. An antibody specific for POT1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPOT1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for POT1 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 POT1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : POT1 is a member of the telombin family and encodes a nuclear protein involved in telomere maintenance. Specifically, this protein functions as a member of a m µLti-protein complex that binds to the TTAGGG repeats of telomeres, reg µLating telomere length and protecting chromosome ends from illegitimate recombination, catastrophic chromosome instability, and abnormal chromosome segregation. Increased transcriptional expression of this gene is associated with stomach carcinogenesis and its progression. Alternatively spliced transcript variants have been described.Human POT1 encodes a 71-kD protein whose N-terminal region shares 26% identity with the N terminus of S. pombe Pot1. POT1 is a housekeeping gene required to ensure the integrity of chromosome ends in all cells.
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 : Chicken (Gallus)
UniProt :
Abbreviation : PSMB7
Alternative Names : RP11-101K10.7; Z; macropain chain Z|m µLticatalytic endopeptidase complex chain Z|proteasome beta 7 subunit|proteasome catalytic subunit 2|proteasome subunit Z|proteasome subunit alpha|proteasome sub
Application :
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV :
Inter-AssayCV :
Recovery :
Sample Type : Serum, Plasma, Other biological fluids
Detection Method :
Analysis Method?? :
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Product Overview :
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Species Reactivity : Chicken (Gallus)
UniProt : P27607
Abbreviation : PTGS2
Alternative Names : COX-2; COX2; GRIPGHS; PGG/HS; PGHS-2; PHS-2; hCox-2; cyclooxygenase 2b|prostaglandin G/H synthase and cyclooxygenase|prostaglandin-endoperoxide synthase 2
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?6.7%
Inter-AssayCV : ?9.3%
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 PTGS2 in samples. An antibody specific for PTGS2 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPTGS2 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PTGS2 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 PTGS2 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : Cyclooxygenase (COX) enzymes catalyze the synthesis of prostaglandins (PGs) from arachidonic acid. There are two isoforms of COX, COX-1 and COX-2. While COX-1 is expressed constitutively and appears to be responsible for the production of prostaglandins (PGs) that control normal physiologic functions, expression of COX-2 is induced by various inflammatory and mitogenic stim µLi such as cytokines, growth factors or tumor promoters. Numerous experimental studies s µggest a relationship between COX-2 expression and carcinogenesis. For example, increased amounts of COX-2 have been observed in breast cancers that overexpress HER-2/neu. Furthermore, treatment with selective inhibitors of COX-2 reduced the formation of tongue, esophagal, intestinal, breast, skin, lung, and bladder tumors in experimental animals.
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 : Chicken (Gallus)
UniProt : N/A
Abbreviation : PGF2a
Alternative Names : PGF2A; PGF2-A; PG-F2a
Application : ELISA
Range : 9.88-800 pg/mL
Sensitivity : 3.88 pg/mL
Intra-AssayCV : ?5.8%
Inter-AssayCV : ?8.9%
Recovery : 0.93
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 PGF2a in samples. An antibody specific for PGF2a has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPGF2a present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PGF2a 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 PGF2a bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : One of the prostaglandins, a group of hormone-like substances that participate in a wide range of body functions such as the contraction and relaxation of smooth muscle, the dilation and constriction of blood vessels, control of blood pressure, and mod µLation of inflammation. Prostaglandin F2-alpha(PGF-2 alpha) is a stable prostaglandin that stim µLates the contraction of uterine and bronchial smooth muscle and produces vasoconstriction (tightening) in some blood vessels. As a pharmaceutical, the generic name of PGF-2 alpha is dinoprost. It is used for the induction of abortion, for evacuation of the uterus after a missed abortion, and in the treatment of hydatidiform mole.
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 : Chicken (Gallus)
UniProt : O13035
Abbreviation : PSAP
Alternative Names : FLJ00245; GLBA; MGC110993; SAP1; sphingolipid activator protein-1
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?3.8%
Inter-AssayCV : ?8.4%
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 PSAP in samples. An antibody specific for PSAP has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPSAP present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PSAP 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 PSAP bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : Prosaposin also known as PSAP is a highly conserved glycoprotein which is a precursor for 4 cleavage products : saposins A, B, C, and D. Saposin is an acronym for Sphingolipid Activator PrO[S]teINs. Each domain of the precursor protein is approximately 80 amino acid residues long with nearly identical placement of cysteine residues and glycosylation sites. Saposins A-D localize primarily to the lysosomal compartment where they facilitate the catabolism of glycosphingolipids with short oligosaccharide groups. The precursor protein exists both as a secretory protein and as an integral membrane protein and has neurotrophic activities.Saposins A-D are required for the hydrolysis of certain shingolipids by specific lysosomal hydrolases.
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 : Chicken (Gallus)
UniProt :
Abbreviation : PROM1
Alternative Names : AC133; CD133; CORD12; MCDR2; MSTP061; PROML1; RP41; STGD4; hProminin|hematopoietic stem cell antigen|prominin-like 1
Application :
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV :
Inter-AssayCV :
Recovery :
Sample Type : Serum, Plasma, Other biological fluids
Detection Method :
Analysis Method?? :
Test principle :
Product Overview :
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Species Reactivity : Chicken (Gallus)
UniProt : Q5ZKL5
Abbreviation : PREPL
Alternative Names : FLJ16627; KIAA0436; OTTHUMP00000202420|OTTHUMP00000202421|OTTHUMP00000202424|OTTHUMP00000202425|OTTHUMP00000202426|putative prolyl oligopeptidase
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?4.9%
Inter-AssayCV : ?7.8%
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 PREPL in samples. An antibody specific for PREPL has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPREPL present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PREPL 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 PREPL bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : PREPL belongs to the prolyl oligopeptidase subfamily of serine peptidases. Mutations in this gene have been associated with hypotonia-cystinuria syndrome, also known as the 2p21 deletion syndrome. Several alternatively spliced transcript variants encoding either the same or different isoforms have been described for this gene. The longest deduced protein contains 727 amino acids and has a propeller domain in its N-terminal half and a catalytic domain, including the catalytic triad (ser, asp, his) essential for serine peptidases, in its C-terminal half. In sharp contrast to PREP and oligopeptidase B, which require both amino- and carboxy-terminal sequences for activity, PREPL activity appeared to depend only on the carboxy-terminal domain.
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 : Chicken (Gallus)
UniProt : Q6JHU7
Abbreviation : LEPREL1
Alternative Names : FLJ10718; MLAT4; P3H2; myxoid liposarcoma associated protein 4|prolyl 3-hydroxylase 2|prolyl 3-hydroxylase 3
Application : ELISA
Range : 0.312-20 ng/mL
Sensitivity : 0.126 ng/mL
Intra-AssayCV : ?3.9%
Inter-AssayCV : ?7.2%
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 LEPREL1 in samples. An antibody specific for LEPREL1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyLEPREL1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for LEPREL1 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 LEPREL1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : LEPREL1 belongs to a family of collagen prolyl hydroxylases required for proper collagen biosynthesis, folding, and assembly. The deduced 708-amino acid protein has an N-terminal signal peptide, 4 tetratricopeptide repeats, 4 CxxxC motifs, a central leucine zipper, a prolyl 4-hydroxylase-alpha domain, which contains an ATP/GTP-binding site, and a C-terminal endoplasmic retic µLum (ER) retention motif (KDEL). LEPREL1 also has 3 potential N-glycosylation sites and putative glycosaminoglycan attachment sites. It shares 53% and 45% amino acid identity with LEPRE1 and LEPRE2, respectively. Northern blot analysis detected weak expression of a 3.4-kb transcript in most tissues examined, with higher levels in placenta and kidney. A 6.5-kb transcript was expressed abundantly in skeletal muscle and more weakly in heart.
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 : Q9DEA3
Species : Chicken
Former Code :
Alias : MGC8367, DNA polymerase delta auxiliary protein|cyclin
Product Type : ELISA Kit
Sample Type : serum, plasma, tissue homogenates, cell lysates
Detect Range : 3.12 ng/ml-200 ng/ml
Sensitivity : 0.78 ng/ml
Antigen Name : proliferating cell nuclear antigen
Abbreviation : PCNA
Protein Biological Process 1 : Transcription/Transcription reg µLation
Protein Biological Process 2 :
Protein Biological Process 3 : DNA replication
Assay Time : 1-5h
Sample Volume : 50-100 µL
Detection Wavelength : 450 nm
Delievery Date : 5-7 working days

Species Reactivity : Chicken (Gallus)
UniProt : P14676
Abbreviation : PRLR
Alternative Names : hPRLrI; delta 4-SF1b truncated prolactin receptor|delta 4-delta 7/11 truncated prolactin receptor|hPRL receptor|prolactin receptor delta 7/11|secreted prolactin binding protein
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?7.3%
Inter-AssayCV : ?9.9%
Recovery : 0.86
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 PRLR in samples. An antibody specific for PRLR has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPRLR present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PRLR 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 PRLR bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : The prolactin receptor—encoded by a gene on Chromosome 5p13-14—interacts with the prolactin molec µLe as a transmembrane receptor.The 5-prime-untranslated region of the PRLR gene contains 2 alternative first exons : E13, the human counterpart of the rat and mouse E13, and a novel human type of alternative first exon termed E1N. The 5-prime-untranslated region also contains a common noncoding exon 2 and part of exon 3, which contains the translation initiation codon. The E13 and E1N exons are within 800 basepairs of each other. These 2 exons are expressed in human breast tissue, breast cancer cells, gonads, and liver. Overall, the transcript containing E13 is prevalent in most tissues. The PRLR gene product is encoded by exons 3-10, of which exon 10 encodes most of the intracell µLar domain.
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 : Chicken (Gallus)
UniProt : Q04594
Abbreviation : PRL
Alternative Names : LTH; Luteotropic Hormone
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?4.1%
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 PRL in samples. An antibody specific for PRL has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPRL present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for PRL 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 PRL bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : Luteotropic hormone is a peptide hormone discovered by Dr. Henry Friesen, primarily associated with lactation. In breastfeeding, the act of an infant suckling the nipple stim µLates the production of prolactin, which fills the breast with milk via a process called lactogenesis, in preparation for the next feed. Oxytocin, another hormone, is also released, which triggers milk let-down.Prolactin (PRL) is a peptide hormone primarily associated with lactation. In breastfeeding, the infant suckling the teat stim µLates the production of prolactin, which fills the breast with milk (lactogenesis) in preparation for the next feed. Oxytocin, a similar hormone, is also released, which triggers milk let-down. Prolactin (PRL) is a polypeptide hormone secreted by anterior pituitary of both male and female.
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).