Rapid Mouse Ig Isotyping Array 1
RayBio® Rapid Mouse Immunoglobulin Isotyping Array 1. Detects 8 Mouse Ig sub-classes and 2 light chain types. Suitable for serum, plasma, and cell culture supernatants.User Manual
|Product Category:||Isotyping Arrays|
|Semi- / Quantitative:||Semi-Quantitative|
|Solid Support:||Glass Slide|
|Detection Method:||Fluorescence Laser Scanner|
|Number of targets:||10|
Compatible Sample Types
Cell Culture Supernatants, Plasma, Serum, Tissue Lysates, Cell Lysates
IgA, IgD, IgE, IgM, IgG1, IgG2a, IgG2b, and IgG3 Heavy Chains; Kappa and Lambda Light Chains
- One step mouse monoclonal antibody isotyping
- Use only 1-2 µl sample
- The whole experiment can be done within 1 hour
- Sandwich based technology for high specificity and sensitivity
- Low system CV with high reproducibility
- High throughput sample processing
- Qualitative visual inspection or semi-quantitative result
- Processed slides can be stored for years without signal decay
Isotyping; Monoclonal Antibody Development; Hybridoma Screening and Selection; Biomarker Screening; Confirming Biological Processes
Free Antibody Array Analysis Tool & Array Scanning Service
All RayBio antibody array kits are supported by a free Excel-based analysis tool particular to each array for the automatic computation of the extracted numerical data obtained from the array image. Features include automated sorting and averaging, background subtraction, normalization, data plotting as well as advanced computations for quantitative arrays. Also antibody lists, array maps and .gal files with the individual layout of each array are available.
In case you do not have access to a compatible laser scanner a scanning service for all RayBio glass slide antibody arrays can be offered for free. Only shipping charges apply.
Please contact us by email, phone or using this form for further details.
- Groscurth S et al. (2012) Artificial forisomes are ideal models of forisome assembly and activity that allow the development of technical devices. Biomacromolecules 13(10):3076-86. doi: 10.1021/bm3008499