PCSK1 ELISA Kit (Human) (OKCD00932)
OKCD00932 96 Wells
EUR 997.2
Description: Description of target: Involved in the processing of hormone and other protein precursors at sites comprised of pairs of basic amino acid residues. Substrates include POMC, renin, enkephalin, dynorphin, somatostatin, insulin and AGRP.;Species reactivity: Human;Application: ELISA;Assay info: Assay Methodology: Quantitative Sandwich Immunoassay;Sensitivity: < 0.115 ng/mL

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Human True insulin ELISA kit
1 plate of 96 wells
EUR 822
Description: A competitive ELISA for quantitative measurement of Human True insulin in samples from blood, plasma, serum, cell culture supernatant and other biological fluids. This is a high quality ELISA kit developped for optimal performance with samples from the particular species.

Human True insulin ELISA kit
96 wells plate
EUR 405

Human True insulin ELISA Kit
48-Strip-Wells-(Competitive)
EUR 485

Human True insulin ELISA Kit
48-Strip-Wells-(Sandwich)
EUR 485

Human True insulin ELISA Kit
5x96-Strip-Wells-(Competitive)
EUR 3020

Human True insulin ELISA Kit
96-Strip-Wells-(Competitive)
EUR 690

Human True insulin ELISA Kit
96-Strip-Wells-(Sandwich)
EUR 690

Human Samples information

COMP Chemi-Luminescent ELISA Kit (Human) (OKCD03392)
OKCD03392 96 Wells
EUR 1185.6
Description: Description of target: May play a role in the structural integrity of cartilage via its interaction with other extracellular matrix proteins such as the collagens and fibronectin. Can mediate the interaction of chondrocytes with the cartilage extracellular matrix through interaction with cell surface integrin receptors. Could play a role in the pathogenesis of osteoarthritis. Potent suppressor of apoptosis in both primary chondrocytes and transformed cells. Suppresses apoptosis by blocking the activation of caspase-3 and by inducing the IAP family of survival proteins (BIRC3, BIRC2, BIRC5 and XIAP). Essential for maintaining a vascular smooth muscle cells (VSMCs) contractile/differentiated phenotype under physiological and pathological stimuli. Maintains this phenotype of VSMCs by interacting with ITGA7 .;Species reactivity: Human;Application: ;Assay info: Assay Methodology: Quantitative Sandwich ELISA;Sensitivity: 0.41 ng/mL

OKCD06003-96W - KIT ELISA Kit (Human)
OKCD06003-96W 96Wells
EUR 525

OKCD01291-96W - Complement 1q Antibody ELISA Kit (Human)
OKCD01291-96W 96Wells
EUR 800

AR ELISA Kit (Human) (OKCD00824)
OKCD00824 96 Wells
EUR 950.4

C6 ELISA Kit (Human) (OKCD01158)
OKCD01158 96 Wells
EUR 997.2
Description: Description of target: Constituent of the membrane attack complex (MAC) that plays a key role in the innate and adaptive immune response by forming pores in the plasma membrane of target cells. ;Species reactivity: Human;Application: ELISA;Assay info: Assay Methodology: Quantitative Sandwich Immunoassay;Sensitivity: < 0.294 ng/mL

PC ELISA Kit (Human) (OKCD02783)
OKCD02783 96 Wells
EUR 997.2
Description: Description of target: Pyruvate carboxylase catalyzes a 2-step reaction, involving the ATP-dependent carboxylation of the covalently attached biotin in the first step and the transfer of the carboxyl group to pyruvate in the second. Catalyzes in a tissue specific manner, the initial reactions of glucose (liver, kidney) and lipid (adipose tissue, liver, brain) synthesis from pyruvate. ;Species reactivity: Human;Application: ;Assay info: Assay Methodology: Quantitative Sandwich ELISA;Sensitivity: 0.55 ng/mL

F2 ELISA Kit (Human) (OKCD06709)
OKCD06709 96 Wells
EUR 903.6
Description: Description of target: Coagulation factor II is proteolytically cleaved to form thrombin in the first step of the coagulation cascade which ultimately results in the stemming of blood loss. F2 also plays a role in maintaining vascular integrity during development and postnatal life.Coagulation factor II is proteolytically cleaved to form thrombin in the first step of the coagulation cascade which ultimately results in the stemming of blood loss. F2 also plays a role in maintaining vascular integrity during development and postnatal life. Mutations in F2 leads to various forms of thrombosis and dysprothrombinemia. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.;Species reactivity: Human;Application: ELISA;Assay info: ;Sensitivity: < 0.35ng/mL

C7 ELISA Kit (Human) (OKCD06740)
OKCD06740 96 Wells
EUR 903.6
Description: Description of target: This gene encodes a serum glycoprotein that forms a membrane attack complex together with complement components C5b, C6, C8, and C9 as part of the terminal complement pathway of the innate immune system. The protein encoded by this gene contains a cholesterol-dependent cytolysin/membrane attack complex/perforin-like (CDC/MACPF) domain and belongs to a large family of structurally related molecules that form pores involved in host immunity and bacterial pathogenesis. This protein initiates membrane attack complex formation by binding the C5b-C6 subcomplex and inserts into the phospholipid bilayer, serving as a membrane anchor. Mutations in this gene are associated with a rare disorder called C7 deficiency.;Species reactivity: Human;Application: ELISA;Assay info: ;Sensitivity: < 0.4ng/mL

HP ELISA Kit (Human) (OKCD06850)
OKCD06850 96 Wells
EUR 684
Description: Description of target: This gene encodes a preproprotein, which is processed to yield both alpha and beta chains, which subsequently combine as a tetramer to produce haptoglobin. Haptoglobin functions to bind free plasma hemoglobin, which allows degradative enzymes to gain acce;Species reactivity: Human;Application: ELISA;Assay info: ;Sensitivity: < 2.87ng/mL

F9 ELISA Kit (Human) (OKCD06888)
OKCD06888 96 Wells
EUR 903.6
Description: Description of target: This gene encodes vitamin K-dependent coagulation factor IX that circulates in the blood as an inactive zymogen. This factor is converted to an active form by factor XIa, which excises the activation peptide and thus generates a heavy chain and a light chain held together by one or more disulfide bonds. The role of this activated factor IX in the blood coagulation cascade is to activate factor X to its active form through interactions with Ca+2 ions, membrane phospholipids, and factor VIII. Alterations of this gene, including point mutations, insertions and deletions, cause factor IX deficiency, which is a recessive X-linked disorder, also called hemophilia B or Christmas disease. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing.;Species reactivity: Human;Application: ELISA;Assay info: ;Sensitivity: < 32pg/mL

C3 ELISA Kit (Human) (OKCD06920)
OKCD06920 96 Wells
EUR 652.8
Description: Description of target: Complement component C3 plays a central role in the activation of complement system. Its activation is required for both classical and alternative complement activation pathways. The encoded preproprotein is proteolytically processed to generate alpha and beta subunits that form the mature protein, which is then further processed to generate numerous peptide products. The C3a peptide, also known as the C3a anaphylatoxin, modulates inflammation and possesses antimicrobial activity. Mutations in this gene are associated with atypical hemolytic uremic syndrome and age-related macular degeneration in human patients.;Species reactivity: Human;Application: ELISA;Assay info: ;Sensitivity: < 2.8ng/mL

C2 ELISA Kit (Human) (OKCD06923)
OKCD06923 96 Wells
EUR 903.6
Description: Description of target: Component C2 is part of the classical pathway of complement system. Activated C1 cleaves C2 into C2a and C2b. C2a leads to activation of C3. Deficiency of C2 has been reported to associated with certain autoimmune diseases.Component C2 is part of the classical pathway of complement system. Activated C1 cleaves C2 into C2a and C2b. C2a leads to activation of C3. Deficiency of C2 has been reported to associated with certain autoimmune diseases.;Species reactivity: Human;Application: ELISA;Assay info: ;Sensitivity: < 0.291ng/mL

CP ELISA Kit (Human) (OKCD06981)
OKCD06981 96 Wells
EUR 950.4
Description: Description of target: The protein encoded by this gene is a metalloprotein that binds most of the copper in plasma and is involved in the peroxidation of Fe(II)transferrin to Fe(III) transferrin. Mutations in this gene cause aceruloplasminemia, which results in iron accumulation and tissue damage, and is associated with diabetes and neurologic abnormalities. Two transcript variants, one protein-coding and the other not protein-coding, have been found for this gene.;Species reactivity: Human;Application: ELISA;Assay info: ;Sensitivity: < 0.294ng/mL

TH ELISA Kit (Human) (OKCD07395)
OKCD07395 96 Wells
EUR 1123.2
Description: Description of target: The specific function of the protein remains unknown. The protein encoded by this gene is involved in the conversion of tyrosine to dopamine. It is the rate-limiting enzyme in the synthesis of catecholamines, hence plays a key role in the physiology of adrenergic neurons. Mutations in this gene have been associated with autosomal recessive Segawa syndrome. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.;Species reactivity: Human;Application: ELISA;Assay info: ;Sensitivity: < 0.066ng/mL

GC ELISA Kit (Human) (OKCD07681)
OKCD07681 96 Wells
EUR 1123.2
Description: Description of target: Vitamin D binding protein (GC) is the major carrier protein of vitamin D that also transports components such as fatty acids and endotoxins and has an important role in the actin scaveging system. GC is a 52-58 kDa plasma protein synthesized mainly by hepatocytes. Polymorphisms in the gene give rise to three major electrophoretic variants, Gc1, Gc1s and Gc1f that differ by amino acid substitutions as well as glycosylations. The physiological significance of these phenotypes has yet to be determined.;Species reactivity: Human;Application: ELISA;Assay info: ;Sensitivity: < 0.074ng/mL

C9 ELISA Kit (Human) (OKCD07697)
OKCD07697 96 Wells
EUR 1123.2
Description: Description of target: This gene encodes the final component of the complement system. It participates in the formation of the Membrane Attack Complex (MAC). The MAC assembles on bacterial membranes to form a pore, permitting disruption of bacterial membrane organization. Mutations in this gene cause component C9 deficiency.;Species reactivity: Human;Application: ELISA;Assay info: ;Sensitivity: < 2.64ng/mL

F7 ELISA Kit (Human) (OKCD07755)
OKCD07755 96 Wells
EUR 1123.2
Description: Description of target: This gene encodes coagulation factor VII which is a vitamin K-dependent factor essential for hemostasis. This factor circulates in the blood in a zymogen form, and is converted to an active form by either factor IXa, factor Xa, factor XIIa, or thrombin by minor proteolysis. Upon activation of the factor VII, a heavy chain containing a catalytic domain and a light chain containing 2 EGF-like domains are generated, and two chains are held together by a disulfide bond. In the presence of factor III and calcium ions, the activated factor then further activates the coagulation cascade by converting factor IX to factor IXa and/or factor X to factor Xa. Alternative splicing of this gene results in 2 transcripts. Defects in this gene can cause coagulopathy.;Species reactivity: Human;Application: ELISA;Assay info: ;Sensitivity: < 3.4pg/mL