Anti-MHC II DR-alpha + beta chain antibody [Bra30] (STJ16101040)

SPECIFICATIONS
ClonalityMonoclonal
HostMouse
ConjugationUnconjugated
IsotypeIgG2ak
ImmunogenA BALB/c mouse was immunized with REH (human ALL cell line). Fusion partner: SP-2/0.
STJ16101040
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General Information

Short DescriptionMouse monoclonal anti-MHC II DR-alpha + beta chain for use in FC and IHC in Human samples. Datasheet included with dilution recommendations, and related reagents.
ApplicationsFC/IHC
HostMouse
ReactivityHuman
NoteSTRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT TO BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.

Product Properties

ClonalityMonoclonal
Clone IDBra30
IsotypeIgG2ak
ConjugationUnconjugated
ConcentrationCan be provided as 100 ยตg/mL, 500 ยตg/mL or 1mg/mL.
PurificationAffinity purified from tissue culture.
Dilution RangeFlow cytometry (0, 5-1, 0 ยตg/million cells in 0, 1 ml). Immunohistology (1-2 ยตg/ml for 30 min at RT; staining of formalin-fixed tissues requires boiling tissue sections in 10mM citrate buffer, pH 6.0, for 10-20 min followed by cooling at RT for 20 mi
FormulationPBS with 0.02% Sodium Azide.
Storage InstructionStore for up to 1 year at 2-8ยฐC upon receipt.

Target Information

ImmunogenA BALB/c mouse was immunized with REH (human ALL cell line). Fusion partner: SP-2/0.

Additional Info

Background MHC class II molecules are encoded by polymorphic MHC genes and consist of a non-covalent complex of an Alpha and Beta chain. Helper T lymphocytes bind antigenic peptides presented by MHC class II molecules. MHC class II molecules bind 13-18 amino acid antigenic peptides. Accumulating in endosomal/lysosomal compartments and on the surface of B cells, HLA-DM and-DO molecules regulate binding of exogenous peptides to class II molecules (HLA-DR) by sustaining a conformation that favors peptide exchange. The differential structural properties of MHC class I and class II molecules account for their respective roles in activating different populations of T lymphocytes.

Information sourced from Uniprot.org

Citations

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