Suitable for WB, ELISA, ICC/IF. Preadsorbed to minimise non-specific binding and high background staining.
Goat
Mouse
IgM
Mu chain
Human
APC
Ex: 650nm, Em: 660nm
WB, ELISA, ICC/IF
Polyclonal
Application | Reactivity | Dilution info | Notes |
---|---|---|---|
Application WB | Reactivity Reacts | Dilution info - | Notes - |
Application ELISA | Reactivity Reacts | Dilution info - | Notes - |
Application ICC/IF | Reactivity Reacts | Dilution info 0.1 µg for 106 Cells | Notes - |
Constant region of immunoglobulin heavy chains. Immunoglobulins, also known as antibodies, are membrane-bound or secreted glycoproteins produced by B lymphocytes. In the recognition phase of humoral immunity, the membrane-bound immunoglobulins serve as receptors which, upon binding of a specific antigen, trigger the clonal expansion and differentiation of B lymphocytes into immunoglobulins-secreting plasma cells. Secreted immunoglobulins mediate the effector phase of humoral immunity, which results in the elimination of bound antigens (By similarity). The antigen binding site is formed by the variable domain of one heavy chain, together with that of its associated light chain. Thus, each immunoglobulin has two antigen binding sites with remarkable affinity for a particular antigen. The variable domains are assembled by a process called V-(D)-J rearrangement and can then be subjected to somatic hypermutations which, after exposure to antigen and selection, allow affinity maturation for a particular antigen (By similarity).Isoform 1Constant region of secreted IgM (sIgM), also known as the Fc region of IgM antibody. Able to multimerize, forms high order polymers, mainly pentamers and occasionally hexamers, providing for multivalency and high avidity recognition of antigens (By similarity). Natural sIgM are polyreactive and recognize conserved self- and pathogen-derived structures, whereas immune sIgM are secreted only upon exposure to pathogens and are antigen-specific. Both natural and immune sIgM are required for an efficient humoral immune response to infection (PubMed:10899913, PubMed:28135254, PubMed:34788614). Mediates sIgM effector functions mostly via Fc receptors and the complement system. On lymphoid cells binds high-affinity Fc receptor FCMR and promotes induction of an efficient neutralizing IgG response while maintaining tolerance to self-antigens. Recruits C1q complement component to initiate the classical complement pathway, facilitating the recognition and neutralization of pathogens by the host. Together with C1q and mannose-binding lectin promotes the phagocytosis of apoptotic cells by macrophages, ensuring the clearance of potential autoimmune epitopes from tissues (By similarity) (PubMed:10899913, PubMed:11062505, PubMed:28135254). Involved in mucosal immunity. It is transported by transcytosis across mucosal epithelium by PIGR and secreted on the apical side in complex with PIGR secretory component to scan mucosal lining for pathogens. IgM-antigen complexes undergo FCMR-mediated retrotranscytosis across mucosal M cells toward antigen-presenting cells in mucosal lymphoid tissues (PubMed:34788614).Isoform 2Constant region of membrane-bound IgM, part of the B cell receptor complex (BCR). IgM BCR provides constitutive tonic signaling for B cell survival. Mediates pre-BCR signaling that regulates B cell selection and rearrangement of Ig genes via allelic exclusion.
Igh-6, Igh-6, Ighm, Immunoglobulin heavy constant mu
Suitable for WB, ELISA, ICC/IF. Preadsorbed to minimise non-specific binding and high background staining.
Goat Anti-Mouse IgM mu chain (APC) preadsorbed
Goat
Mouse
IgM
Mu chain
Human
APC
Ex: 650nm, Em: 660nm
WB, ELISA, ICC/IF
Polyclonal
Yes
ab130780 reacts with the heavy chain of mouse IgM. Goat Anti-Mouse IgM mu chain (Allophycocyanin) preadsorbed shows minimal cross reactivity with Human immunoglobulins.
IgG
Liquid
pH: 7.3
Preservative: 0.1% Sodium azide
Constituents: PBS, Sucrose
ab130780 is purified by affinity chromatography on mouse IgM covalently linked to agarose.
Blue Ice
+4°C
+4°C
Store in the dark
ab130780 is preadsorbed against Mouse IgG1, IgG2a, IgG2b, IgG3 and IgA, pooled Human sera and purified Human paraproteins.
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ELISA plate was coated with purified mouse IgM, IgG, and IgA. Immunoglobulins were detected with serially diluted ab130780.
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