Human SRANKL ELISA Kit |
EHS0291 |
Abclonal |
96Tests |
EUR 625.2 |
Human Elisa Laboratories manufactures the ampli srankl human elisa reagents distributed by Genprice. The Ampli Srankl Human Elisa reagent is RUO (Research Use Only) to test human serum or cell culture lab samples. To purchase these products, for the MSDS, Data Sheet, protocol, storage conditions/temperature or for the concentration, please contact Human elisa. Other Ampli products are available in stock. Specificity: Ampli Category: Srankl Group: Human Elisa
Anserini SRANKL ELISA Kit |
Abclonal |
96Tests |
EUR 625.2 |
Bovine SRANKL ELISA Kit |
Abclonal |
96Tests |
EUR 625.2 |
Canine SRANKL ELISA Kit |
Abclonal |
96Tests |
EUR 625.2 |
Goat SRANKL ELISA Kit |
Abclonal |
96Tests |
EUR 625.2 |
Human true insulin,TI ELISA Kit |
SunredBio |
96 tests |
EUR 528 |
|
Description: A quantitative ELISA kit for measuring Human in samples from biological fluids. |
Human true insulin,TI ELISA Kit |
ChemNorm |
96T |
EUR 567.6 |
Human Elisa information
sRANKL antibody (biotin) |
60R-RG003bt |
Fitzgerald |
50 ug |
EUR 457.2 |
Description: Goat polyclonal sRANKL antibody (biotin) conjugated |
Human sRANKL Flow Cytometry Assay - Group 5 |
HX88811 |
Antigenix America |
96 Tests |
EUR 270 |
sRANKL Recombinant Protein |
40-699 |
ProSci |
2 ug |
EUR 311.1 |
Description: RANKL and RANK are members of the TNF superfamily of ligands and receptors that play an important role in the regulation of specific immunity and bone turnover. RANK (receptor) was originally identified as a dendritic cell-membrane protein, which, by interacting with RANKL, augments the ability of dendritic cells. These dendritic cells then stimulate naïve T-cell proliferation in a mixed lymphocyte reaction, promote the survival of RANK+ T-cells, and regulate T-cell-dependent immune response. RANKL, which is expressed in a variety of cells, including osteoblasts, fibroblasts, activated T-cells and bone marrow stromal cells, is also capable of interacting with a decoy receptor called OPG. Binding of soluble OPG to sRANKL inhibits osteoclastogenesis by interrupting the signaling between stromal cells and osteoclastic progenitor cells, thereby leading to excess accumulation of bone and cartilage. Recombinant Murine sRANK Ligand is a 19.8 kDa polypeptide comprising the TNF-homologous region of RANKL (178 amino acid residues). |
sRANKL Human, Soluble RANK Ligand Human Recombinant Protein, GST tag |
PROTO14788-1 |
BosterBio |
Regular: 10ug |
EUR 380.4 |
Description: RANKL Human Recombinant fused to GST tag produced in E.Coli is a single, non-glycosylated polypeptide having a molecular mass of 47 kDa. ;RANKL is purified by proprietary chromatographic techniques. |
sRANKL Human, Soluble RANK Ligand Human Recombinant Protein, His Tag |
PROTO14788-2 |
BosterBio |
Regular: 20ug |
EUR 380.4 |
Description: sRANKL Human Recombinant produced in E.Coli is a single, non-glycosylated polypeptide chain containing 199 amino acids (140-317 a.a) and having a molecular mass of 22.3kDa.;sRANKL is fused to a 21 amino acid His-tag at N-terminus & purified by proprietary chromatographic techniques. |
Human sRANKL(SolubleReceptor Activator of Nuclear factor-kB Ligand) ELISA Kit |
ELK2646-48T |
ELK Biotech |
48T |
Ask for price |
|
Description: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human sRANKL. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human sRANKL. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human sRANKL, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Human sRANKL in the samples is then determined by comparing the OD of the samples to the standard curve. |
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