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AB150123

Goat Anti-Mouse IgM mu chain (Alexa Fluor® 647)

5

(1 Review)

|

(25 Publications)

Suitable for ELISA, IHC-Fr, IHC-P, Flow Cyt, ICC/IF. Ideal for fluorescent cell and tissue imaging. Cited in 25 publications.

View Alternative Names

Igh-6, Ighm, Immunoglobulin heavy constant mu

2 Images
Immunocytochemistry/ Immunofluorescence - Goat Anti-Mouse IgM mu chain (Alexa Fluor® 647) (AB150123)
  • ICC/IF

Lab

Immunocytochemistry/ Immunofluorescence - Goat Anti-Mouse IgM mu chain (Alexa Fluor® 647) (AB150123)

ICC/IF image of ab20346 stained HeLa cells. The cells were 4% formaldehyde fixed (10 min), permeabilized with 0.1% Triton X-100 for 5 minutes and then incubated in 1% BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab20346, 1/500) overnight at +4°C. The secondary antibody (red) was ab150123 used at 2µg/ml for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.

The negative control (inset) is a secondary-only assay to demonstrate low non-specific binding of the secondary antibody.

Alexa Fluor® - Goat Anti-Mouse IgM mu chain (Alexa Fluor® 647) (AB150123)
  • Alexa Fluor®

Unknown

Alexa Fluor® - Goat Anti-Mouse IgM mu chain (Alexa Fluor® 647) (AB150123)

Key facts

Host species

Goat

Target species

Mouse

Target isotype

IgM

Target specificity

Mu chain

Minimal cross-reactivity
Pre-adsorbed

No

Conjugation

Alexa Fluor® 647

Excitation/Emission

Ex: 650nm, Em: 665nm

Applications

IHC-Fr, ICC/IF, Flow Cyt, IHC-P, ELISA

applications

Clonality

Polyclonal

Isotype

IgG

Reactivity data

{ "title": "Reactivity Data", "filters": { "stats": ["", "Reactivity", "Dilution Info", "Notes"] }, "values": { "ELISA": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p></p>" }, "IHC-Fr": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p></p>" }, "IHC-P": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p></p>" }, "Flow Cyt": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"1/2000", "notes":"<p></p>" }, "ICC/IF": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"1-2 µg/mL", "notes":"<p></p>" } } }

Product details

Alexa Fluor® is a registered trademark of Molecular Probes, Inc, a Thermo Fisher Scientific Company. The Alexa Fluor® dye included in this product is provided under an intellectual property license from Life Technologies Corporation. As this product contains the Alexa Fluor® dye, the purchase of this product conveys to the buyer the non-transferable right to use the purchased product and components of the product only in research conducted by the buyer (whether the buyer is an academic or for-profit entity). As this product contains the Alexa Fluor® dye the sale of this product is expressly conditioned on the buyer not using the product or its components, or any materials made using the product or its components, in any activity to generate revenue, which may include, but is not limited to use of the product or its components: in manufacturing; (ii) to provide a service, information, or data in return for payment (iii) for therapeutic, diagnostic or prophylactic purposes; or (iv) for resale, regardless of whether they are sold for use in research. For information on purchasing a license to this product for purposes other than research, contact Life Technologies Corporation, 5781 Van Allen Way, Carlsbad, CA 92008 USA or outlicensing@thermofisher.com.

Properties and storage information

Form
Liquid
Purification technique
Affinity purification Immunogen
Purification notes
Antiserum was solid phase adsorbed to ensure class specificity. This antibody was isolated by affinity chromatography using antigen coupled to agarose beads.
Storage buffer
Preservative: 0.02% Sodium azide Constituents: PBS, 23% Glycerol (glycerin, glycerine), 1% BSA
Shipped at conditions
Blue Ice
Appropriate short-term storage duration
1-2 weeks
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C
Aliquoting information
Upon delivery aliquot
Storage information
Avoid freeze / thaw cycle|Stable for 12 months at -20°C|Store in the dark

Product protocols

Target data

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 1. Constant 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 2. Constant 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.
See full target information Ighm

Publications (25)

Recent publications for all applications. Explore the full list and refine your search

Frontiers in immunology 16:1576917 PubMed40735312

2025

Cryofibrinogen-associated glomerulonephritis with paraproteinemia.

Applications

Unspecified application

Species

Unspecified reactive species

Xuanli Tang,Mengya Jiang,Huaqin Zhang,Peng Bi,Jun Wang,Tian Ye,Jie Zheng,Mengli Tong,Xingyu Zhu,Xiaotao Hou,Shuhua Bao,Yi Lin,Xue Jiang,Hongyu Chen,Feng Wan,Haichun Yang

Methods in molecular biology (Clifton, N.J.) 2924:101-112 PubMed40307638

2025

Induced Pluripotent Stem Cell-Derived Retinal Pigment Epithelial Cells for the Study of Macular Degeneration.

Applications

Unspecified application

Species

Unspecified reactive species

Almar Neiteler,Shyamanga Borooah,James A Ross

Nature communications 16:3429 PubMed40210885

2025

Genetic modulation of rare earth nanoparticle biotransformation shapes biological outcomes.

Applications

Unspecified application

Species

Unspecified reactive species

Mingming Tian,Di Wu,Xiao Gou,Ruibin Li,Xiaowei Zhang

Biological & pharmaceutical bulletin 48:151-161 PubMed39993746

2025

Involvement of the Na/Ca Exchanger in the Automaticity of the Cardiomyocytes from the Guinea Pig Pulmonary Vein but Not the Sinus Node.

Applications

Unspecified application

Species

Unspecified reactive species

Ryosuke Odaka,Kana Sekiguchi,Shogo Hamaguchi,Iyuki Namekata,Hikaru Tanaka

Cell death & disease 15:745 PubMed39394145

2024

High mitochondrial DNA content is a key determinant of stemness, proliferation, cell migration, and cancer metastasis in vivo.

Applications

Unspecified application

Species

Unspecified reactive species

Marta Mauro-Lizcano,Filippo Di Pisa,Luis Larrea Murillo,Conor J Sugden,Federica Sotgia,Michael P Lisanti

Brain communications 6:fcae256 PubMed39130515

2024

appear resistant to trans-synaptic tau propagation.

Applications

Unspecified application

Species

Unspecified reactive species

James H Catterson,Edmond N Mouofo,Inés López De Toledo Soler,Gillian Lean,Stella Dlamini,Phoebe Liddell,Graham Voong,Taxiarchis Katsinelos,Yu-Chun Wang,Nils Schoovaerts,Patrik Verstreken,Tara L Spires-Jones,Claire S Durrant

MedComm 5:e514 PubMed38495123

2024

Transcriptomic analysis of rat brain response to alternating current electrical stimulation: unveiling insights via single-nucleus RNA sequencing.

Applications

Unspecified application

Species

Unspecified reactive species

Yan Wang,Yongchao Ma,Qiuling Zhong,Bing Song,Qian Liu

Nature structural & molecular biology 31:568-577 PubMed38347148

2024

Single-nucleoid architecture reveals heterogeneous packaging of mitochondrial DNA.

Applications

Unspecified application

Species

Unspecified reactive species

R Stefan Isaac,Thomas W Tullius,Katja G Hansen,Danilo Dubocanin,Mary Couvillion,Andrew B Stergachis,L Stirling Churchman

Development, growth & differentiation 66:248-255 PubMed38326088

2024

Dissection of N-deacetylase and N-sulfotransferase activities of NDST1 and their effects on Wnt8 distribution and signaling in Xenopus embryos.

Applications

Unspecified application

Species

Unspecified reactive species

Minako Suzuki,Shinji Takada,Yusuke Mii

Nanoscale 15:16277-16286 PubMed37650749

2023

Nitrogen-functionalized graphene quantum dot incorporated GelMA microgels as fluorescent 3D-tissue Constructs.

Applications

Unspecified application

Species

Unspecified reactive species

Aida Zahra Taravatfard,Carlos Ceballos-Gonzalez,Abu Bakar Siddique,Johana Bolivar-Monsalve,Masoud Madadelahi,Grissel Trujillo-de Santiago,Mario Moisés Alvarez,Ashit Kumar Pramanick,Eduardo Martinez Guerra,Lawrence Kulinsky,Marc J Madou,Sergio O Martinez,Mallar Ray
View all publications

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