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Immunofluorescence analysis of Goat anti-Mouse IgG1 Secondary Antibody, Alexa Fluor 555 conjugate (Produce # A21127) was performed using HeLa cells stained with alpha Tubulin (236-10501) Mouse Monoclonal Antibody (Product # A11126). The cells were fixed with 4% paraformaldehyde for 10 minutes, permeabilized with 0.1% Triton™ X-100 for 10 minutes, blocked with 1% BSA for 1 hour and labeled with mouse primary antibody (1:250 dilution) for 3 hours at room temperature. Goat anti-Mouse IgG1 Secondary Antibody, Alexa Fluor 555 conjugate was used at concentration of 2 µg/ml in phosphate buffered saline containing 0.2 % BSA for 45 minutes at room temperature, for detection of alpha Tubulin in the cytoplasm (Panel a: green). Nuclei (Panel b: blue) were stained with DAPI in SlowFade® Gold Antifade Mountant (Product # S36938). F-actin was stained with Alexa Fluor® 488 Phalloidin (Product # A12379, 1:300) (Panel c: red). Panel d represents the composite image. No nonspecific staining was observed with the secondary antibody alone (panel f), or with an isotype control (panel e). The images were captured at 60X magnification.
|Tested species reactivity||Mouse|
|Published species reactivity||Not Applicable|
|Host / Isotype||Goat / IgG|
|Immunogen||IgG gamma 1|
|Conjugate||Alexa Fluor® 555|
|Storage buffer||PBS, pH 7.5|
|Contains||5mM sodium azide|
|Storage Conditions||4° C, store in dark|
|Cross Adsorption||Against mouse IgM, mouse IgA, pooled human sera, purified human paraproteins and mouse isotypes IgG2a, IgG2b and IgG3 prior to conjugation|
|Antibody Form||Whole Antibody|
|Tested Applications||Dilution *|
|Flow Cytometry (Flow)||1:500|
|Immunocytochemistry (ICC)||2 µg/ml|
|Immunofluorescence (IF)||1-10 µg/mL|
|Immunohistochemistry (IHC)||1-10 µg/ml|
* Suggested working dilutions are given as a guide only. It is recommended that the user titrate the product for use in their own experiment using appropriate negative and positive controls.
To minimize cross-reactivity, these goat anti-mouse IgG1 whole secondary antibodies have been affinity purified and cross-adsorbed against mouse IgM, mouse IgA, pooled human sera, purified human paraproteins, and mouse isotypes IgG2a, IgG2b, and IgG3 prior to conjugation. Cross-adsorption or pre-adsorption is a purification step to increase specificity of the antibody resulting in higher sensitivity and less background staining. The secondary antibody solution is passed through a column matrix containing immobilized serum proteins from potentially cross-reactive species. Only the nonspecific-binding secondary antibodies are captured in the column, and the highly specific secondaries flow through. The benefits of this extra step are apparent in multiplexing/multicolor-staining experiments (e.g., flow cytometry) where there is potential cross-reactivity with other primary antibodies or in tissue/cell fluorescent staining experiments where there are may be the presence of endogenous immunoglobulins.
Alexa Fluor dyes are among the most trusted fluorescent dyes available today. Invitrogen™ Alexa Fluor 555 dye is a bright, orange-fluorescent dye with excitation ideally suited to the 555 nm laser line. For stable signal generation in imaging and flow cytometry, Alexa Fluor 555 dye is pH-insensitive over a wide molar range. Probes with high fluorescence quantum yield and high photostability allow detection of low-abundance biological structures with great sensitivity. Alexa Fluor 555 dye molecules can be attached to proteins at high molar ratios without significant self-quenching, enabling brighter conjugates and more sensitive detection. The degree of labeling for each conjugate is typically 2-8 fluorophore molecules per IgG molecule; the exact degree of labeling is indicated on the certificate of analysis for each product lot.
Using conjugate solutions: Centrifuge the protein conjugate solution briefly in a microcentrifuge before use; add only the supernatant to the experiment. This step will help eliminate any protein aggregates that may have formed during storage, thereby reducing nonspecific background staining. Because staining protocols vary with application, the appropriate dilution of antibody should be determined empirically. For the fluorophore-labeled antibodies a final concentration of 1-10 µg/mL should be satisfactory for most immunohistochemistry and flow cytometry applications.
We offer an extensive line of Invitrogen™ secondary antibody conjugates with well-characterized specificity and labeled with a wide selection of premium fluorescent dyes, including Invitrogen™ Alexa Fluor™ fluorescent dyes. Fluorescent secondary antibody conjugates are useful in the detection, sorting, or purification of its specified target and ideal for fluorescence microscopy and confocal laser scanning microscopy, flow cytometry, and fluorescent western detection. The breadth of fluorescent markers we offer allows our reagents to be tailored to almost any fluorescent detection system.
Secondary antibodies may be provided in three formats: whole IgG, divalent F(ab')2 fragments, and monovalent Fab fragments. Because of the high degree of conservation in the structure of many immunoglobulin domains, most class-specific secondary antibodies must be affinity-purified and cross-adsorbed to achieve minimal cross-reaction with other immunoglobulins.
Our secondary antibody conjugates are most commonly prepared by immunizing the host animal with a pooled population of immunoglobulins from the target species and can be further purified and modified (e.g., immunoaffinity chromatography, antibody fragmentation, label conjugation, etc.) to generate highly specific reagents. In the first round of purification, whole immunoglobulins binding to the immunizing antibody are recovered and mainly consist of the ~150-kDa IgG class. Further purification, for example, with Protein A or G, removes all unwanted immunoglobulin classes except the affinity-purified antibodies that react with the target-specific immunoglobulin heavy and/or light chains.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
|Not Applicable||Not Cited||Binding of a sialic acid-recognizing lectin Siglec-9 modulates adhesion dynamics of cancer cells via calpain-mediated protein degradation.||Sabit I,Hashimoto N,Matsumoto Y,Yamaji T,Furukawa K,Furukawa K||The Journal of biological chemistry (288:35417)||2013|
|Not Applicable||Not Cited||Adenosine and dopamine receptors coregulate photoreceptor coupling via gap junction phosphorylation in mouse retina.||Li H,Zhang Z,Blackburn MR,Wang SW,Ribelayga CP,O'Brien J||The Journal of neuroscience : the official journal of the Society for Neuroscience (33:3135)||2013|
|Not Applicable||Not Cited||Gangliosides play pivotal roles in the regulation of complement systems and in the maintenance of integrity in nerve tissues.||Ohmi Y,Tajima O,Ohkawa Y,Mori A,Sugiura Y,Furukawa K,Furukawa K||Proceedings of the National Academy of Sciences of the United States of America (106:22405)||2009|
|Not Applicable||Not Cited||Expanding the multicolor capabilities of basic confocal microscopes by employing red and near-infrared quantum dot conjugates.||Kingeter LM,Schaefer BC||BMC biotechnology (9:null)||2009|
|Not Applicable||Not Cited||Human protein factory for converting the transcriptome into an in vitro-expressed proteome,.||Goshima N,Kawamura Y,Fukumoto A,Miura A,Honma R,Satoh R,Wakamatsu A,Yamamoto J,Kimura K,Nishikawa T,Andoh T,Iida Y,Ishikawa K,Ito E,Kagawa N,Kaminaga C,Kanehori K,Kawakami B,Kenmochi K,Kimura R,Kobayashi M,Kuroita T,Kuwayama H,Maruyama Y,Matsuo K,Minami K,Mitsubori M,Mori M,Morishita R,Murase A,Nishikawa A,Nishikawa S,Okamoto T,Sakagami N,Sakamoto Y,Sasaki Y,Seki T,Sono S,Sugiyama A,Sumiya T,Takayama T,Takayama Y,Takeda H,Togashi T,Yahata K,Yamada H,Yanagisawa Y,Endo Y,Imamoto F,Kisu Y,Tanaka S,Isogai T,Imai J,Watanabe S,Nomura N||Nature methods (5:1011)||2008|
|Not Applicable||Not Cited||Multiple immunofluorescence labelling of formalin-fixed paraffin-embedded (FFPE) tissue.||Robertson D,Savage K,Reis-Filho JS,Isacke CM||BMC cell biology (9:null)||2008|
|Not Applicable||Not Cited||Calcineurin localization in skeletal muscle offers insights into potential new targets.||Torgan CE,Daniels MP||The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society (54:119)||2006|
|Not Applicable||Not Cited||
The long non-coding RNA nuclear-enriched abundant transcript 1_2 induces paraspeckle formation in the motor neuron during the early phase of amyotrophic lateral sclerosis.
A-21127 was used in immunocytochemistry to analyze paraspeckle formation in the motor neuron during the early phase of amyotrophic lateral sclerosis induced by the long non-coding RNA nuclear-enriched abundant transcript 1_2
|Nishimoto Y,Nakagawa S,Hirose T,Okano HJ,Takao M,Shibata S,Suyama S,Kuwako K,Imai T,Murayama S,Suzuki N,Okano H||Molecular brain (6:null)||2013|