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  • Mouse Anti-Rabbit Light Chain-HRP (SB62a-R - Recombinant)

Mouse Anti-Rabbit Light Chain-HRP (SB62a-R - Recombinant)

Cat. No.:
24060-05
HRP Anti-Rabbit Light Chain recombinant antibody for use in ELISA and western blot assays.
$176.00
Size Price (USD) Quantity
0.5 mL $176.00
Technical Bulletin Safety Datasheet

Product Specifications

More Information
Clone SB62a-R
(Genetically derived from DNA sequences of a parental hybridoma clone; for details on the parental clone, see Cat. No. 4060)
Isotype Mouse (BALB/c) IgG2bλ
Isotype Control Mouse IgG2b-HRP (A-1)
Specificity Rabbit light chains
Immunogen Rabbit light chains
Conjugate HRP (Horseradish Peroxidase)
Buffer Formulation 50% Glycerol/50% Phosphate buffered saline, pH 7.4
Clonality Monoclonal
Concentration Lot specific
Volume 0.5 mL
Recommended Storage 2-8°C
Applications ELISA – Quality tested
Western Blot – Quality tested

Documentation

Documentation
Technical Bulletin Safety Datasheet
Certificate of Analysis Lookup

Enter the Catalog Number and Lot Number for the Certificate of Analysis you wish to view


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  1. Paraffin embedded human gastric cancer tissue was stained with Mouse IgG<sub>2b</sub>-HRP isotype control (SB Cat. No. 0104-05; left) and Mouse Anti-Cytokeratin 18-HRP (SB Cat. No. 10085-05; right) followed by DAB and hematoxylin.
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  2. ELISA plate was coated with purified rabbit IgG and IgM. Immunoglobulins were detected with serially diluted Goat F(ab')<sub>2</sub> Anti-Rabbit IgG(H+L), Mouse/Rat/Human ads-HRP (SB Cat. No. 4054-05).
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  3. Total cell lysates from Jurkat cells were resolved by electrophoresis, transferred to PVDF membrane, and probed with Rabbit Anti-Human DR5-UNLB (SB Cat. No. 6600-01). Proteins were visualized using Goat Anti-Rabbit IgG(H+L), Mouse/Human ads-HRP (SB Cat. No. 4050-05) secondary antibody and chemiluminescent detection.
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  4. Rabbit IgG-UNLB (SB Cat. No. 0111-01) was resolved by electrophoresis, transferred to PVDF membrane, and visualized using Goat Anti-Rabbit IgG-HRP (SB Cat. No. 4030-05) secondary antibody and chemiluminescent detection.
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  5. ELISA plate was coated with purified rabbit IgG and IgM. Immunoglobulins were detected with Swine Anti-Rabbit IgG(H+L), Mouse/Rat/Human/Goat SP ads-HRP (SB Cat. No. 6310-05).
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  6. ELISA plate was coated with purified rabbit IgM and IgG. Immunoglobulins were detected with serially diluted Goat Anti-Rabbit IgM-HRP (SB Cat. No. 4020-05).
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  7. Lysates from mouse embryonic fibroblasts expressing no Bak (Bax-/-Bak-/- (DKO)), mouse Bak (Bax-/-), or WT human Bak (in DKO) were resolved by electrophoresis, transferred to nitrocellulose membrane, and probed with anti-Bak followed by Goat Anti-Rabbit Ig, Human ads-HRP (SB Cat. No. 4010-05) and chemiluminescent detection.<br/>Image from Alsop AE, Fennell SC, Bartolo RC, Tan IK, Dewson G, Kluck RM. Dissociation of Bak α1 helix from the core and latch domains is required for apoptosis. Nat Commun. 2015;6:6841. Figure 1(a)
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  8. Paraffin embedded sections of mouse P8 testes were stained with anti-BCAS2 and anti-PLZF. The DNA was stained with Hoechst 33342 and mounted with Fluoromount-G<sup>&reg;</sup> (SB Cat. No. 0100-01).<br/>Images from Liu W, Wang F, Xu Q, Shi J, Zhang X, Liu X, et al. BCAS2 is involved in alternative mRNA splicing in spermatogonia and the transition to meiosis. Nat Commun. 2017;8:14182. Figure 1(d)<br/>Reproduced under the Creative Commons license https://creativecommons.org/licenses/by/4.0/
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  9. ELISA plate was coated with purified rabbit IgG Fc and IgG Fab. Immunoglobulins were detected with serially diluted Goat Anti-Rabbit IgG Fc-HRP (SB Cat. No. 4041-05).
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  10. ELISA plate was coated with purified rabbit IgG and IgM. Immunoglobulins were detected with serially diluted Goat Anti-Rabbit IgG-HRP (SB Cat. No. 4030-05).
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  13. ELISA plate was coated with serially diluted Rabbit IgM-UNLB (SB Cat. No. 0113-01). Immunoglobulin was detected with Goat Anti-Rabbit IgG-BIOT (SB Cat. No. 4030-08) and Goat Anti-Rabbit IgM-BIOT (SB Cat. No. 4020-08) followed by Streptavidin-HRP (SB Cat No. 7100-05) and quantified.
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  14. ELISA plate was coated with purified rabbit IgG and IgM. Immunoglobulins were detected with serially diluted Goat Anti-Rabbit IgG(H+L), Mouse/Rat/Human ads-HRP (SB Cat. No. 4049-05).
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  15. Lane 1 - Rabbit IgG<br/>Lane 2 - Rabbit IgG Light Chains<br/>Lane 3 - Rabbit IgG Heavy Chains<br/>Rabbit immunoglobulins above were resolved by electrophoresis under reducing conditions, transferred to PVDF membrane, and probed with Mouse Anti-Rabbit IgG-HRP (SB Cat. No. 4090-05). Proteins were visualized using chemiluminescent detection.
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  19. ELISA plate was coated with serially diluted Rabbit F(ab')<sub>2</sub> IgG-UNLB (SB Cat. No. 0112-01). Immunoglobulin was detected with Goat Anti-Rabbit IgG F(ab')<sub>2</sub>-BIOT and Goat Anti-Rabbit IgG Fc-BIOT (SB Cat. No. 4041-08) followed by Streptavidin-HRP (SB Cat No. 7100-05) and quantified.
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  20. RNA helicase A (RHA) positive and normal human serum was resolved by electrophoresis, transferred to nitrocellulose membrane, and probed with anti-RHA followed by Goat F(ab')<sub>2</sub> Anti-Rabbit IgG(H+L), Mouse/Human ads-HRP (SB Cat. No. 4052-05) and chemiluminescent detection.<br/>Image from Vázquez-Del Mercado M, Palafox-Sánchez CA, Muñoz-Valle JF, Orozco-Barocio G, Oregon-Romero E, Navarro-Hernández RE, et al. High prevalence of autoantibodies to RNA helicase A in Mexican patients with systemic lupus erythematosus. Arthritis Res Ther. 2010;12:R6. Figure 1(b)<br/>Reproduced under the Creative Commons license https://creativecommons.org/licenses/by/2.0/
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