Skip to main content Skip to navigation
PE Rat Anti-Mouse CD98
PE Rat Anti-Mouse CD98
Flow cytometric analysis of CD98 expression on unstimulated or Con A-stimulated mouse splenocytes. BALB/c mouse splenic leucocytes were tested fresh (Unstimulated; Left Panel) or 48 hours after Con A mitogenic stimulation (Stimulated; Right Panel). The cells were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody (Mouse BD Fc Block™) (Cat. No. 553141/553142) and stained with either PE Rat IgG2a, κ Isotype Control (Cat. No. 553930; dotted line histogram) or PE Rat Anti-Mouse CD98 antibody (Cat No. 567949; solid line histogram) at 0.125 µg/test. The fluorescence histograms showing CD98 expression (or Ig Isotype control staining) were derived from gated events with the forward and side light-scatter characteristics of viable mouse leucocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa™ X-20 Cell Analyzer System equipped with a Yellow-Green Laser and FlowJo™ software. Data shown on this Technical Data Sheet are not lot specific.
Flow cytometric analysis of CD98 expression on unstimulated or Con A-stimulated mouse splenocytes. BALB/c mouse splenic leucocytes were tested fresh (Unstimulated; Left Panel) or 48 hours after Con A mitogenic stimulation (Stimulated; Right Panel). The cells were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody (Mouse BD Fc Block™) (Cat. No. 553141/553142) and stained with either PE Rat IgG2a, κ Isotype Control (Cat. No. 553930; dotted line histogram) or PE Rat Anti-Mouse CD98 antibody (Cat No. 567949; solid line histogram) at 0.125 µg/test. The fluorescence histograms showing CD98 expression (or Ig Isotype control staining) were derived from gated events with the forward and side light-scatter characteristics of viable mouse leucocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa™ X-20 Cell Analyzer System equipped with a Yellow-Green Laser and FlowJo™ software. Data shown on this Technical Data Sheet are not lot specific.
Product Details
Down Arrow Up Arrow


BD Pharmingen™
Slc3a2; Cd98; 4F2; 4F2HC; CD98 heavy chain; Ly-10; Ly-m10; Ly10
Mouse (QC Testing)
Rat OFA, also known as Outbred OFA IgG2a, κ
EL4-6.1 Thymoma Cells
Flow cytometry (Routinely Tested)
0.2 mg/ml
Aqueous buffered solution containing ≤0.09% sodium azide.
RUO


Preparation And Storage

Store undiluted at 4°C and protected from prolonged exposure to light. Do not freeze. The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography. The antibody was conjugated to the dye under optimum conditions and unconjugated antibody and free dye were removed.

Recommended Assay Procedures

BD® CompBeads can be used as surrogates to assess fluorescence spillover (Compensation). When fluorochrome conjugated antibodies are bound to BD® CompBeads, they have spectral properties very similar to cells. However, for some fluorochromes there can be small differences in spectral emissions compared to cells, resulting in spillover values that differ when compared to biological controls. It is strongly recommended that when using a reagent for the first time, users compare the spillover on cells and BD CompBeads to ensure that BD® CompBeads are appropriate for your specific cellular application.

Product Notices

  1. Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
  2. Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.
  3. For fluorochrome spectra and suitable instrument settings, please refer to our Multicolor Flow Cytometry web page at www.bdbiosciences.com/colors.
  4. Please refer to http://regdocs.bd.com to access safety data sheets (SDS).
  5. Since applications vary, each investigator should titrate the reagent to obtain optimal results.
  6. An isotype control should be used at the same concentration as the antibody of interest.
567949 Rev. 1
Antibody Details
Down Arrow Up Arrow
RL388

The RL388 monoclonal antibody recognizes CD98 which is also known as the 4F2 antigen and Ly-10. CD98 is a disulfide-linked heterodimer comprised of an ~86 kDa single-pass type II heavy chain glycoprotein that associates with a ~39-kDa multi-pass, nonglycosylated light chain which belongs to the L-type amino transporter family. The RL388 antibody specifically binds to an epitope present on the CD98 heavy chain (CD98hc, also known as the 4F2 cell-surface antigen heavy chain or 4F2hc) which is encoded by Slc3a2 [solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2]. CD98 is variably expressed on different cell types including T cells, B cells, and NK cells as well as monocytes, granulocytes, platelets, and fibroblasts. CD98 serves as an activation marker for T and B cells since its expression is upregulated upon cellular activation. CD98 regulates cellular growth, proliferation, and survival through CD98hc interactions with β integrins and by CD98 light chain-mediated amino acid transport.

        

567949 Rev. 1
Format Details
Down Arrow Up Arrow
PE
R-Phycoerythrin (PE), is part of the BD family of Phycobiliprotein dyes. This fluorochrome is a multimeric fluorescent phycobiliprotein with excitation maximum (Ex Max) of 496 nm and 566 nm and an emission maximum (Em Max) at 576 nm. PE is designed to be excited by the Blue (488 nm), Green (532 nm) and Yellow-Green (561 nm) lasers and detected using an optical filter centered near 575 nm (e.g., a 575/26-nm bandpass filter). As PE is excited by multiple lasers, this can result in cross-laser excitation and fluorescence spillover on instruments with various combinations of Blue, Green, and Yellow-Green lasers. Please ensure that your instrument’s configurations (lasers and optical filters) are appropriate for this dye.
altImg
PE
Yellow-Green 488 nm, 532 nm, 561 nm
496 nm, 566 nm
576 nm
567949 Rev.1
Citations & References
Down Arrow Up Arrow
View product citations for antibody "567949" on CiteAb

Development References (7)

  1. Cantor J, Browne CD, Ruppert R, et al. CD98hc facilitates B cell proliferation and adaptive humoral immunity. Nat Immunol. 2009; 10(4):412-419. (Clone-specific: Flow cytometry). View Reference
  2. Cantor JM, Ginsberg MH. CD98 at the crossroads of adaptive immunity and cancer. J Cell Sci. 2012; 125(Pt 6):1373-1382. (Biology). View Reference
  3. Ernst DN, McQuitty DN, Weigle WO, Hobbs MV. Expression of membrane activation antigens on murine B lymphocytes stimulated with lipopolysaccharide. Cell Immunol. 1988; 114(1):161-173. (Clone-specific: Flow cytometry). View Reference
  4. Ernst DN, Weigle WO, McQuitty DN, Rothermel AL, Hobbs MV. Stimulation of murine T cell subsets with anti-CD3 antibody. Age-related defects in the expression of early activation molecules. J Immunol. 1989; 142(5):1413-1421. (Clone-specific: Flow cytometry). View Reference
  5. Luscher B, Rousseaux M, Lees R, MacDonald HR, Bron C. Cell surface glycoproteins involved in the stimulation of interleukin 1-dependent interleukin 2 production by a subline of EL4 thymoma cells. II. Structure, biosynthesis, and maturation. J Immunol. 1985; 135(6):3951-3957. (Clone-specific: Immunoprecipitation, Radioimmunoassay). View Reference
  6. MacDonald HR, Lees RK, Bron C. Cell surface glycoproteins involved in the stimulation of interleukin 1-dependent interleukin 2 production by a subline of EL4 thymoma cells. I. Functional characterization by monoclonal antibodies. J Immunol. 1985; 135(6):3944-3950. (Immunogen: (Co)-stimulation, Flow cytometry, Functional assay, Radioimmunoassay). View Reference
  7. Sato Y, Heimeier RA, Li C, Deng C, Shi YB. Extracellular domain of CD98hc is required for early murine development.. Cell Biosci. 2011; 1(1):7. (Biology). View Reference
View All (7) View Less
567949 Rev. 1

Please refer to Support Documents for Quality Certificates


Global - Refer to manufacturer's instructions for use and related User Manuals and Technical data sheets before using this products as described


Comparisons, where applicable, are made against older BD Technology, manual methods or are general performance claims.  Comparisons are not made against non-BD technologies, unless otherwise noted.

For Research Use Only. Not for use in diagnostic or therapeutic procedures.