ELISA/assay

Rat Resolvin E2 ELISA Kit

MBS020304

48-Strip-Wells

470 USD

ELISA Kit

Rat Resolvin E2 ELISA Kit

[Resolvin E2]

[cyclophilin, partial; Peptidyl-prolyl cis-trans isomerase B; peptidyl-prolyl cis-trans isomerase B; PPIase B; rotamase B; S-cyclophilin; cyclophilin-like protein; peptidylprolyl isomerase B (cyclophilin B); CYP-S1; Cyclophilin B; Rotamase B; S-cyclophilin]

[RvE2]

[PPIB; PPIB; OI9; CYPB; SCYLP; CYP-S1; CYPB; PPIase B; SCYLP]

PPIB_HUMAN

Rat

No significant cross-reactivity or interference between this analyte and analogues is observed.

Store all reagents at 2-8 degree C

Samples: Rabbit Body Fluids And Tissue Homogenates. Assay Type: Quantitative Sandwich. Detection Range: 31.2pg/ml-1000pg/ml. Sensitivity: 5.0pg/ml.

Intra-assay Precision: Intra-assay CV (%) is less than 15%. Inter-assay Precision: Inter-assay CV (%) is less than 15%. [CV(%) = SD/mean ×100]. All CV% should be compared by concentration, not compared by OD values.

Background/Introduction: This Quantitative Sandwich ELISA kit is for lab reagent/research use only, not for drug, household, therapeutic or diagnostic applications! This kit is intended to be used for determine the level of RvE2 (hereafter termed "analyte") in undiluted original Rabbit body fluids and tissue homogenates. This kit is NOT suitable for assaying non-biological sources of substances.

181250

AAA35733.1

P23284

23,743 Da

Collagen Biosynthesis And Modifying Enzymes Pathway (645289); Collagen Formation Pathway (645288); Extracellular Matrix Organization Pathway (576262); Prolactin Signaling Pathway (672462); Syndecan-1-mediated Signaling Events Pathway (138046)

The protein encoded by this gene is a cyclosporine-binding protein and is mainly located within the endoplasmic reticulum. It is associated with the secretory pathway and released in biological fluids. This protein can bind to cells derived from T- and B-lymphocytes, and may regulate cyclosporine A-mediated immunosuppression. Variants have been identified in this protein that give rise to recessive forms of osteogenesis imperfecta. [provided by RefSeq, Oct 2009]

PPIB: PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides. Defects in PPIB are the cause of osteogenesis imperfecta type 9 (OI9). OI9 is a connective tissue disorder characterized by bone fragility, low bone mass and bowing of limbs due to multiple fractures. Short limb dwarfism and blue sclerae are observed in some but not all patients. Belongs to the cyclophilin-type PPIase family. PPIase B subfamily. Protein type: Secreted, signal peptide; Secreted; Cyclophilin; Isomerase; EC 5.2.1.8; RNA-binding; Chaperone. Chromosomal Location of Human Ortholog: 15q21-q22. Cellular Component: focal adhesion; smooth endoplasmic reticulum; membrane; perinuclear region of cytoplasm; endoplasmic reticulum; endoplasmic reticulum lumen; melanosome; nucleus. Molecular Function: collagen binding; protein binding; peptidyl-prolyl cis-trans isomerase activity; unfolded protein binding; protein complex binding; peptide binding. Biological Process: extracellular matrix organization and biogenesis; protein peptidyl-prolyl isomerization; protein stabilization; positive regulation of multicellular organism growth. Disease: Osteogenesis Imperfecta, Type Ix

48-Strip-Wells

470 USD

96-Strip-Wells

680

5x96-Strip-Wells

3100

10x96-Strip-Wells

6095