Mouse IgG1, kappa monoclonal [MOPC-21] - isotype control Cited in 55 publications.
IgG1
Mouse
pH: 7.2
Preservative: 0.09% Sodium azide
Constituents: PBS
Liquid
Monoclonal
Application | Reactivity | Dilution info | Notes |
---|---|---|---|
Application IP | Reactivity Expected | Dilution info - | Notes - |
Application IHC-Fr | Reactivity Expected | Dilution info - | Notes - |
Application WB | Reactivity Expected | Dilution info - | Notes - |
Application IHC-P | Reactivity Expected | Dilution info - | Notes - |
Application Flow Cyt | Reactivity Expected | Dilution info - | Notes Suitable for surface or intracellular staining. |
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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 (PubMed:22158414, PubMed:20176268). 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 (PubMed:17576170, PubMed:20176268).
Immunoglobulin heavy constant gamma 4, Ig gamma-4 chain C region, IGHG4
Mouse IgG1, kappa monoclonal [MOPC-21] - isotype control Cited in 55 publications.
Immunoglobulin heavy constant gamma 4, Ig gamma-4 chain C region, IGHG4
IgG1
Mouse
pH: 7.2
Preservative: 0.09% Sodium azide
Constituents: PBS
Liquid
Monoclonal
MOPC-21
Affinity purification Protein G
MOPC-21 immunoglobulin has unknown specificity and was chosen as an isotype control after screening on a variety of resting, activated, live and fixed rat and human tissues.
kappa
Blue Ice
+4°C
ab18443 MOPC-21 immunoglobulin is useful as an isotype-matched control in Western blotting, immunoprecipitation, immunohistochemical staining, bioassay and immunofluorescent staining (surface or intracellular) for flow cytometric analysis.
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Terms & Conditions.
SH3GL1/Endophilin A2 was immunoprecipitated from 0.35 mg Rat brain tissue lysate with Anti-SH3GL1/Endophilin A2 antibody [K51/1] ab317835 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using Anti-SH3GL1/Endophilin A2 antibody [K51/1] ab317835 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(VeriBlot for IP Detection Reagent (HRP) ab131366) was used at 1/5000 dilution.
Lane 1: Rat brain tissue lysate
Lane 2: Anti-SH3GL1/Endophilin A2 antibody [K51/1] ab317835 IP in Rat brain tissue lysate
Lane 3: Mouse monoclonal IgG (ab18443) instead of Anti-SH3GL1/Endophilin A2 antibody [K51/1] ab317835 in rat testis tissue lysate
All lanes: Immunoprecipitation - Anti-SH3GL1/Endophilin A2 antibody [K51/1] (Anti-SH3GL1/Endophilin A2 antibody [K51/1] ab317835) at 1/30 dilution
All lanes: Rat brain tissue lysate at 0.35 mg
All lanes: Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (VeriBlot for IP Detection Reagent (HRP) ab131366) at 1/5000 dilution
Exposure time: 41s
SH3GL1/Endophilin A2 was immunoprecipitated from 0.35 mg Rat testis tissue lysate with Anti-SH3GL1/Endophilin A2 antibody [K51/1] ab317835 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using Anti-SH3GL1/Endophilin A2 antibody [K51/1] ab317835 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(VeriBlot for IP Detection Reagent (HRP) ab131366) was used at 1/5000 dilution.
Lane 1: Rat testis tissue lysate
Lane 2: Anti-SH3GL1/Endophilin A2 antibody [K51/1] ab317835 IP in Rat testis tissue lysate
Lane 3: Mouse monoclonal IgG (ab18443) instead of Anti-SH3GL1/Endophilin A2 antibody [K51/1] ab317835 in rat testis tissue lysate
All lanes: Immunoprecipitation - Anti-SH3GL1/Endophilin A2 antibody [K51/1] (Anti-SH3GL1/Endophilin A2 antibody [K51/1] ab317835) at 1/30 dilution
All lanes: Rat testis tissue lysate
All lanes: Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (VeriBlot for IP Detection Reagent (HRP) ab131366) at 1/5000 dilution
Exposure time: 41s
Histone H3 was immunoprecipitated from 0.35 mg NIH/3T3 (mouse embryonic fibroblast) whole cell lysate with Anti-Histone H3 antibody [1B1B2] ab309551 at 1/50 dilution (2ug in 0.4mg lysates). Western blot was performed on the immunoprecipitate using Anti-Histone H3 antibody [1B1B2] ab309551 at 1/1000 dilution. mouse IgG for IP (HRP) (Anti-mouse IgG for IP (HRP) ab131368) was used at 1/5000 dilution.
Lane 1: NIH/3T3 (mouse embryonic fibroblast) whole cell lysate
Lane 2: Anti-Histone H3 antibody [1B1B2] ab309551 IP in NIH/3T3 (mouse embryonic fibroblast) whole cell lysate
Lane 3: Mouse IgG1 monoclonal isotype control (ab18443) instead of Anti-Histone H3 antibody [1B1B2] ab309551 in NIH/3T3 whole cell lysate
Blocking and dilution buffer and concentration: 5% NFDM/TBST.
Exposure time: 32 seconds
All lanes: Immunoprecipitation - Anti-Histone H3 antibody [1B1B2] (Anti-Histone H3 antibody [1B1B2] ab309551) at 1/50 dilution
All lanes: NIH/3T3 (mouse embryonic fibroblast) whole cell lysate
All lanes: Immunoprecipitation - Anti-mouse IgG for IP (HRP) (Anti-mouse IgG for IP (HRP) ab131368) at 1/5000 dilution
Exposure time: 32s
Histone H3 was immunoprecipitated from 0.35 mg C6 (rat glial tumor glial cell) whole cell lysate with Anti-Histone H3 antibody [1B1B2] ab309551 at 1/50 dilution (2ug in 0.4mg lysates). Western blot was performed on the immunoprecipitate using Anti-Histone H3 antibody [1B1B2] ab309551 at 1/1000 dilution. mouse IgG for IP (HRP) (Anti-mouse IgG for IP (HRP) ab131368) was used at 1/5000 dilution.
Lane 1: C6 (rat glial tumor glial cell) whole cell lysate
Lane 2: Anti-Histone H3 antibody [1B1B2] ab309551 IP in C6 (rat glial tumor glial cell) whole cell lysate
Lane 3: Mouse IgG1 monoclonal isotype control (ab18443) instead of Anti-Histone H3 antibody [1B1B2] ab309551 in C6 whole cell lysate
Blocking and dilution buffer and concentration: 5% NFDM/TBST.
Exposure time: 67 seconds
All lanes: Immunoprecipitation - Anti-Histone H3 antibody [1B1B2] (Anti-Histone H3 antibody [1B1B2] ab309551) at 1/50 dilution
All lanes: C6 (rat glial tumor glial cell) whole cell lysate at 10 µg
All lanes: Immunoprecipitation - Anti-mouse IgG for IP (HRP) (Anti-mouse IgG for IP (HRP) ab131368) at 1/5000 dilution
Exposure time: 67s
Histone H3 was immunoprecipitated from 0.35 mg HeLa (human cervical adenocarcinoma epithelial cell) whole cell lysate with Anti-Histone H3 antibody [1B1B2] ab309551 at 1/50 dilution (2ug in 0.4mg lysates). Western blot was performed on the immunoprecipitate using Anti-Histone H3 antibody [1B1B2] ab309551 at 1/1000 dilution. mouse IgG for IP (HRP) (Anti-mouse IgG for IP (HRP) ab131368) was used at 1/5000 dilution.
Lane 1: HeLa (human cervical adenocarcinoma epithelial cell) whole cell lysate
Lane 2: Anti-Histone H3 antibody [1B1B2] ab309551 IP in HeLa (human cervical adenocarcinoma epithelial cell) whole cell lysate
Lane 3: Mouse IgG1 monoclonal isotype control (ab18443) instead of Anti-Histone H3 antibody [1B1B2] ab309551 in HeLa whole cell lysate
Blocking and dilution buffer and concentration: 5% NFDM/TBST.
Exposure time: 32 seconds
All lanes: Immunoprecipitation - Anti-Histone H3 antibody [1B1B2] (Anti-Histone H3 antibody [1B1B2] ab309551) at 1/50 dilution
All lanes: HeLa (human cervical adenocarcinoma epithelial cell) whole cell lysate
All lanes: Immunoprecipitation - Anti-mouse IgG for IP (HRP) (Anti-mouse IgG for IP (HRP) ab131368) at 1/5000 dilution
Exposure time: 32s
CP2c was immunoprecipitated from 0.35 mg C6 (rat glial tumor glial cell) whole cell lysate 10 ug with Anti-CP2c antibody [14/LSF] ab308611 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using Anti-CP2c antibody [14/LSF] ab308611 at 1/1000 dilution. Peroxidase-Conjugated Goat anti-Mouse IgG (H+L) was used at 1/10000 dilution.
Lane 1: C6 (rat glial tumor glial cell) whole cell lysate
Lane 2: Anti-CP2c antibody [14/LSF] ab308611 IP in C6 (rat glial tumor glial cell) whole cell lysate
Lane 3: Mouse monoclonal IgG (ab18443) instead of Anti-CP2c antibody [14/LSF] ab308611 in C6 whole cell lysate
Blocking and dilution buffer and concentration: 5% NFDM/TBST.
Exposure time: 59 seconds
All lanes: Immunoprecipitation - Anti-CP2c antibody [14/LSF] (Anti-CP2c antibody [14/LSF] ab308611) at 1/30 dilution
All lanes: C6 (rat glial tumor glial cell) whole cell lysate
All lanes: Peroxidase-Conjugated Goat anti-Mouse IgG (H+L) at 1/10000 dilution
Exposure time: 59s
CP2c was immunoprecipitated from 0.35 mg Hepa1-6 (mouse hepatoma epithelial cell) whole cell lysate 10 ug with Anti-CP2c antibody [14/LSF] ab308611 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using Anti-CP2c antibody [14/LSF] ab308611 at 1/1000 dilution. Peroxidase-Conjugated Goat anti-Mouse IgG (H+L) was used at 1/10000 dilution.
Lane 1: Hepa1-6 (mouse hepatoma epithelial cell) whole cell lysate
Lane 2: Anti-CP2c antibody [14/LSF] ab308611 IP in Hepa1-6 (mouse hepatoma epithelial cell) whole cell lysate
Lane 3: Mouse monoclonal IgG (ab18443) instead of Anti-CP2c antibody [14/LSF] ab308611 in Hepa1-6 whole cell lysate
Blocking and dilution buffer and concentration: 5% NFDM/TBST.
Exposure time: 59 seconds
All lanes: Immunoprecipitation - Anti-CP2c antibody [14/LSF] (Anti-CP2c antibody [14/LSF] ab308611) at 1/30 dilution
All lanes: Hepa1-6 (mouse hepatoma epithelial cell) whole cell lysate
All lanes: Peroxidase-Conjugated Goat anti-Mouse IgG (H+L) at 1/10000 dilution
Exposure time: 59s
CP2c was immunoprecipitated from 0.35 mg K-562 (human chronic myelogenous leukemia lymphoblast) whole cell lysate 10 ug with Anti-CP2c antibody [14/LSF] ab308611 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using Anti-CP2c antibody [14/LSF] ab308611 at 1/1000 dilution. mouse IgG for IP (HRP) (Anti-mouse IgG for IP (HRP) ab131368) was used at 1/1000 dilution.
Lane 1: K-562 (human chronic myelogenous leukemia lymphoblast) whole cell lysate
Lane 2: Anti-CP2c antibody [14/LSF] ab308611 IP in K-562 (human chronic myelogenous leukemia lymphoblast) whole cell lysate
Lane 3: Mouse monoclonal IgG (ab18443) instead of Anti-CP2c antibody [14/LSF] ab308611 in K-562 whole cell lysate
Blocking and dilution buffer and concentration: 5% NFDM/TBST.
Exposure time: 24 seconds
All lanes: Immunoprecipitation - Anti-CP2c antibody [14/LSF] (Anti-CP2c antibody [14/LSF] ab308611) at 1/30 dilution
All lanes: K-562 (human chronic myelogenous leukemia lymphoblast) whole cell lysate
All lanes: Immunoprecipitation - Anti-mouse IgG for IP (HRP) (Anti-mouse IgG for IP (HRP) ab131368) at 1/1000 dilution
Exposure time: 24s
SHP2 was immunoprecipitated from 0.35 mg NIH/3T3 (mouse embryonic fibroblast) whole cell lysate 10 µg with Anti-SHP2 antibody [79/PTP1D/SHP2] ab290646 at 1/30 dilution (2µg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using Anti-SHP2 antibody [79/PTP1D/SHP2] ab290646 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(VeriBlot for IP Detection Reagent (HRP) ab131366) was used at 1/5000 dilution.
Lane 1: NIH/3T3 (mouse embryonic fibroblast) whole cell lysate 10 µg
Lane 2: Anti-SHP2 antibody [79/PTP1D/SHP2] ab290646 IP in NIH/3T3 whole cell lysate
Lane 3: Mouse IgG1 monoclonal (ab18443) instead of Anti-SHP2 antibody [79/PTP1D/SHP2] ab290646 in NIH/3T3 whole cell lysate
Blocking and dilution buffer and concentration: 5% NFDM/TBST.
Exposure time: 3 seconds
Lane 1: Immunoprecipitation - Anti-SHP2 antibody [79/PTP1D/SHP2] (Anti-SHP2 antibody [79/PTP1D/SHP2] ab290646) at 1/30 dilution
Lane 2: Immunoprecipitation - Anti-SHP2 antibody [79/PTP1D/SHP2] (Anti-SHP2 antibody [79/PTP1D/SHP2] ab290646) at 1/1000 dilution
All lanes: NIH/3T3 (mouse embryonic fibroblast) whole cell lysate at 10 µg
All lanes: Immunoprecipitation - Mouse IgG1, kappa monoclonal [MOPC-21] - isotype control (ab18443) at 1/5000 dilution
Predicted band size: 68 kDa
Exposure time: 3s
Histone H2B was immunoprecipitated from 0.35 mg NIH/3T3 (mouse embryonic fibroblast), whole cell lysate with Anti-Histone H2B antibody [mAbcam 52484] - ChIP Grade ab52484 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using Anti-Histone H2B antibody [mAbcam 52484] - ChIP Grade ab52484 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP) (VeriBlot for IP Detection Reagent (HRP) ab131366) was used at 1/5000 dilution.
Lane 1: NIH/3T3 (mouse embryonic fibroblast), whole cell lysate 10 μg
Lane 2: Anti-Histone H2B antibody [mAbcam 52484] - ChIP Grade ab52484 IP in NIH/3T3 (mouse embryonic fibroblast), whole cell lysate 10 μg
Lane 3: Mouse monoclonal IgG (ab18443) instead of Anti-Histone H2B antibody [mAbcam 52484] - ChIP Grade ab52484 in NIH/3T3 whole cell lysate
Blocking and dilution buffer and concentration: 5% NFDM/TBST.
Exposure time: 32 seconds.
All lanes: Immunoprecipitation - Anti-Histone H2B antibody [mAbcam 52484] - ChIP Grade (Anti-Histone H2B antibody [mAbcam 52484] - ChIP Grade ab52484) at 1/30 dilution
All lanes: NIH/3T3 (mouse embryonic fibroblast), whole cell lysate
All lanes: Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (VeriBlot for IP Detection Reagent (HRP) ab131366) at 1/5000 dilution
Histone H2B was immunoprecipitated from 0.35 mg HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate with Anti-Histone H2B antibody [mAbcam 52484] - ChIP Grade ab52484 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using Anti-Histone H2B antibody [mAbcam 52484] - ChIP Grade ab52484 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(VeriBlot for IP Detection Reagent (HRP) ab131366) was used at 1/5000 dilution.
Lane 1: HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate 10 ug
Lane 2: Anti-Histone H2B antibody [mAbcam 52484] - ChIP Grade ab52484 IP in HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate
Lane 3: Mouse monoclonal IgG (ab18443) instead of Anti-Histone H2B antibody [mAbcam 52484] - ChIP Grade ab52484 in HeLa whole cell lysate
Blocking and dilution buffer and concentration: 5% NFDM/TBST.
Exposure time: 32 seconds.
All lanes: Immunoprecipitation - Anti-Histone H2B antibody [mAbcam 52484] - ChIP Grade (Anti-Histone H2B antibody [mAbcam 52484] - ChIP Grade ab52484) at 1/30 dilution
All lanes: HeLa (human cervix adenocarcinoma epithelial cell), whole cell lysate
All lanes: Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (VeriBlot for IP Detection Reagent (HRP) ab131366) at 1/5000 dilution
Predicted band size: 14 kDa
Observed band size: 15 kDa
p53 was immunoprecipitated from 0.35 mg HEK-293 (human embryonic kidney epithelial cell) whole cell lysate with Anti-p53 antibody [G59-12] ab308609 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using Anti-p53 antibody [G59-12] ab308609 at 1/1000 dilution. mouse IgG for IP (HRP) (Anti-mouse IgG for IP (HRP) ab131368) was used at 1/5000 dilution.
Lane 1: HEK-293 whole cell lysate
Lane 2: Anti-p53 antibody [G59-12] ab308609 IP in HEK-293 whole cell lysate
Lane 3: Mouse IgG1 monoclonal isotype control (ab18443) instead of Anti-p53 antibody [G59-12] ab308609 in HEK-293 whole cell lysate
Blocking and dilution buffer and concentration: 5% NFDM/TBST.
Exposure time: 23 seconds.
The binding pattern observed is consistent with what has been described in the literature (PMID: 31045216; PMID: 16131611).
All lanes: Immunoprecipitation - Anti-p53 antibody [G59-12] (Anti-p53 antibody [G59-12] ab308609) at 1/1000 dilution
All lanes: HEK-293 whole cell lysate at 10 µg
All lanes: Immunoprecipitation - Anti-mouse IgG for IP (HRP) (Anti-mouse IgG for IP (HRP) ab131368) at 1/5000 dilution
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