Mouse TSLP Antibody
R&D Systems, part of Bio-Techne | Catalog # AF555
Key Product Details
Species Reactivity
Validated:
Cited:
Applications
Validated:
Cited:
Label
Antibody Source
Product Specifications
Immunogen
Tyr20-Glu140
Accession # Q9JIE6
Specificity
Clonality
Host
Isotype
Endotoxin Level
Scientific Data Images for Mouse TSLP Antibody
Cell Proliferation Induced by TSLP and Neutralization by Mouse TSLP Antibody.
Recombinant Mouse TSLP (555-TS) stimulates proliferation in the BaF3 mouse pro-B cell line transfected with mouse IL-7 Ra/CD127 in a dose-dependent manner (orange line). Proliferation elicited by Recombinant Mouse TSLP (7.5 ng/mL) is neutralized (green line) by increasing concentrations of Goat Anti-Mouse TSLP Antigen Affinity-purified Polyclonal Antibody (Catalog # AF555). The ND50 is typically ≤0.4 µg/mL.Detection of Mouse TSLP by Immunohistochemistry-Paraffin
Klk5 deletion results in remarkable suppression of the inflammatory phenotype of NS.(A-E). Results show remarkable abrogation of pro-allergic and pro-inflammatory cytokines quantified by RT-qPCR. (A) Il-1 beta, Tslp, Tnf-alpha ; (B) Il-6, Il-18, the type 17 promoting cytokine Il-23p19; (C) Ifn-gamma, Il-4, Il-17A, Il-22; (D) Th17 regulated genes Defb4, Slpi, Cxcl1 and Ccl20; (E) Th17/22 regulated genes s100a7, s100a8, s100a9. Data are shown as the mean ± s.e.m. of triplicate amplification for at least five mice per genotype. Results are normalized to wt mean (set as 1.0). *p<0.05, **p<0.005, ***p<0.001 (Mann-Whitney U test). (F) Quantification of mast cells based on toluidine blue staining of skin tissue (mast cells stain purple). An increased number of mast cells was detected in Spink5-/- dermis; (G) IHC analysis shows abolishment of Tslp expression in Spink5-/-Klk5-/- skin as compared to Spink5-/-; Scale bar: 50μm. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/26390218), licensed under a CC-BY license. Not internally tested by R&D Systems.Detection of Mouse TSLP by Immunohistochemistry-Paraffin
Klk5 deletion results in remarkable suppression of the inflammatory phenotype of NS.(A-E). Results show remarkable abrogation of pro-allergic and pro-inflammatory cytokines quantified by RT-qPCR. (A) Il-1 beta, Tslp, Tnf-alpha ; (B) Il-6, Il-18, the type 17 promoting cytokine Il-23p19; (C) Ifn-gamma, Il-4, Il-17A, Il-22; (D) Th17 regulated genes Defb4, Slpi, Cxcl1 and Ccl20; (E) Th17/22 regulated genes s100a7, s100a8, s100a9. Data are shown as the mean ± s.e.m. of triplicate amplification for at least five mice per genotype. Results are normalized to wt mean (set as 1.0). *p<0.05, **p<0.005, ***p<0.001 (Mann-Whitney U test). (F) Quantification of mast cells based on toluidine blue staining of skin tissue (mast cells stain purple). An increased number of mast cells was detected in Spink5-/- dermis; (G) IHC analysis shows abolishment of Tslp expression in Spink5-/-Klk5-/- skin as compared to Spink5-/-; Scale bar: 50μm. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/26390218), licensed under a CC-BY license. Not internally tested by R&D Systems.Applications for Mouse TSLP Antibody
Western Blot
Sample: Recombinant Mouse TSLP (Catalog # 555-TS)
Neutralization
Formulation, Preparation, and Storage
Purification
Reconstitution
Formulation
Shipping
Stability & Storage
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Background: TSLP
Stromal Lymphopoietin (TSLP) was originally identified from the conditioned medium of a mouse thymic stromal cell line as a protein that promoted the development of B cells. The activity of mouse TSLP overlaps with, but is distinct from, that of mouse IL-7 (1). Mouse TSLP cDNA encodes a 140 amino acid (aa) residue precursor protein with a 19 aa signal sequence. Within the mature region, there are three potential N-glycosylation sites. The Sf 21 cell expressed rmTSLP is likely to be glycosylated at all three sites, as three major glycoforms were visible on SDS-PAGE (Figure 1). Insect cells are known to express relatively simple and homogeneous N-glycans that mainly belong to the high mannose type (2). This recombinant protein was found to be an excellent substrate for N-specific glycosidases such as Endo F3 (Figure 1). The majority of the glycans on rmTSLP can be readily removed by Endo F3. However, a small percentage of the glycans is somewhat resistant to Endo F3 digestion, possibly lacking core fucose, as it is known that core fucosylated N-glycans are strongly preferred substrates for Endo F3 digestion (3).
References
- Sims, J.E. et al. (2000) J. Exp. Med. 192:671.
- Staudacher, E. et al. (1992) Eur. J. Biochem. 207:987.
- Tarentino, A.L. and T.H. Jr. Plummer (1994) Glycobiology 4: 771.
Long Name
Alternate Names
Gene Symbol
UniProt
Additional TSLP Products
Product Documents for Mouse TSLP Antibody
Product Specific Notices for Mouse TSLP Antibody
For research use only