Mouse monoclonal [SB62a] Anti-Rabbit IgG light chain (HRP) (ab99697)

Reviews (1)Q&A (3)References (43)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Mouse monoclonal [SB62a] Anti-Rabbit IgG light chain (HRP) (ab99697)
  • Western blot - Mouse monoclonal [SB62a] Anti-Rabbit IgG light chain (HRP) (ab99697)
  • Western blot - Mouse monoclonal [SB62a] Anti-Rabbit IgG light chain (HRP) (ab99697)
  • Immunoprecipitation - Mouse monoclonal [SB62a] Anti-Rabbit IgG light chain (HRP) (ab99697)
  • Immunoprecipitation - Mouse monoclonal [SB62a] Anti-Rabbit IgG light chain (HRP) (ab99697)
  • Immunoprecipitation - Mouse monoclonal [SB62a] Anti-Rabbit IgG light chain (HRP) (ab99697)
  • Western blot - Mouse monoclonal [SB62a] Anti-Rabbit IgG light chain (HRP) (ab99697)

Key features and details

  • Mouse monoclonal [SB62a] Anti-Rabbit IgG light chain (HRP)
  • Conjugation: HRP
  • Host species: Mouse
  • Isotype: IgG2b
  • Suitable for: IHC-P, ELISA, WB

Overview

  • Product name

    Mouse monoclonal [SB62a] Anti-Rabbit IgG light chain (HRP)
    See all IgG Light chain secondary antibodies

  • Host species

    Mouse

  • Target species

    Rabbit

  • Specificity

    ab99697 reacts with the light chain of native Rabbit IgG primary antibodies and does not bind to the reduced and denatured Rabbit IgG heavy chain band (50kD).

  • Tested applications

    Suitable for: IHC-P, ELISA, WBmore details

  • Immunogen

    Rabbit Light Chain

  • Conjugation

    HRP

Properties

  • Form

    Liquid

  • Storage instructions

    Shipped at 4°C. Store at +4°C.

  • Storage buffer

    pH: 8.2
    Constituents: 50% Glycerol, 50% PBS
  • Concentration information loading...

  • Purity

    Protein A purified

  • Clonality

    Monoclonal

  • Clone number

    SB62a

  • Isotype

    IgG2b

  • Light chain type

    lambda

  • Research areas

Applications

The Abpromise guarantee

Our Abpromise guarantee covers the use of ab99697 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Application Abreviews Notes
IHC-P
1/8000.
ELISA
1/4000 - 1/8000.
WB
Use at an assay dependent concentration.

Note: This antibody is not recommended for sensitive or quantitative detection of the reduced and denatured Rabbit Light Chains on Western Blots.
Notes
IHC-P
1/8000.
ELISA
1/4000 - 1/8000.
WB
Use at an assay dependent concentration.

Note: This antibody is not recommended for sensitive or quantitative detection of the reduced and denatured Rabbit Light Chains on Western Blots.

Images

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Mouse monoclonal [SB62a] Anti-Rabbit IgG light chain (HRP) (ab99697)
    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Mouse monoclonal [SB62a] Anti-Rabbit IgG light chain (HRP) (ab99697)

    IHC image of beta actin staining in human colon formalin fixed paraffin embedded tissue section*. The section was pre-treated using pressure cooker heat mediated antigen retrieval with sodium citrate buffer (pH6) for 30mins. The section was incubated with ab8227, 3µg/ml overnight at +4°C. An HRP-conjugated secondary (ab99697, 1/8000 dilution) was used for 1hr at room temperature. The section was counterstained with haematoxylin and mounted with DPX.

    The inset negative control image is secondary-only at 1/4000 dilution.

    *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre

  • Western blot - Mouse monoclonal [SB62a] Anti-Rabbit IgG light chain (HRP) (ab99697)
    Western blot - Mouse monoclonal [SB62a] Anti-Rabbit IgG light chain (HRP) (ab99697)

    Western blot showing that Mouse monoclonal [SB62a] Secondary Antibody to Rabbit IgG light chain (HRP) (ab99697) specifically binds to light-chains


    Left blot: Coomassie stain showing the rabbit heavy (~50kDa) and light-chains (~25 kDa)

    Lane 1: 10 µg rabbit monoclonal was loaded
    Lane 2: 5 µg rabbit monoclonal was loaded
    Lane 3: 2 µg rabbit monoclonal was loaded

    Right blot: WB using Mouse monoclonal [SB62a] Secondary Antibody to Rabbit IgG light chain (HRP) (ab99697) as secondary antibody at 1/10,000

    Lane 1: 1 µg rabbit monoclonal was loaded
    Lane 2: 0.5 µg rabbit monoclonal was loaded
    Lane 3: 0.25 µg rabbit monoclonal was loaded

  • Western blot - Mouse monoclonal [SB62a] Anti-Rabbit IgG light chain (HRP) (ab99697)
    Western blot - Mouse monoclonal [SB62a] Anti-Rabbit IgG light chain (HRP) (ab99697)
    All lanes : Anti-beta Actin antibody - Loading Control (ab8227) at 1 µg/ml

    Lanes 1-6 : HeLa (Human epithelial carcinoma cell line) Whole Cell Lysate (ab27252)
    Lysates/proteins at 10 µg per lane.

    Secondary
    Lanes 1 - 2 : Mouse monoclonal [SB62a] Secondary Antibody to Rabbit IgG light chain (HRP) (ab99697) at 1/2000 dilution
    Lanes 3 - 4 : Mouse monoclonal [SB62a] Secondary Antibody to Rabbit IgG light chain (HRP) (ab99697) at 1/10000 dilution
    Lanes 5 - 6 : Mouse monoclonal [SB62a] Secondary Antibody to Rabbit IgG light chain (HRP) (ab99697) at 1/20000 dilution

    Developed using the ECL technique.

    Performed under reducing conditions.

  • Immunoprecipitation - Mouse monoclonal [SB62a] Anti-Rabbit IgG light chain (HRP) (ab99697)
    Immunoprecipitation - Mouse monoclonal [SB62a] Anti-Rabbit IgG light chain (HRP) (ab99697)
    LAP2 alpha was immunoprecipitated using 0.5mg Hela whole cell extract, 5µg of Rabbit polyclonal to LAP2 alpha (ab5162)and 50µl of protein G magnetic beads (lane 1). The antibody was incubated with the Protein G beads for 10min under agitation. No antibody was added to the control (lane 2). Hela whole cell extract diluted in RIPA buffer was added to each sample and incubated for 10min under agitation. Proteins were eluted by addition of 40µl SDS loading buffer and incubated for 10min at 70oC; 10µl of each sample was separated on a SDS PAGE gel, transferred to a nitrocellulose membrane, blocked with 5% BSA and probed with ab5162. Secodary: Mouse monoclonal [SB62a] Secondary Antibody to Rabbit IgG light chain (HRP) (ab99697).
    Bands: 83kDa: LAP2 alpha.
  • Immunoprecipitation - Mouse monoclonal [SB62a] Anti-Rabbit IgG light chain (HRP) (ab99697)
    Immunoprecipitation - Mouse monoclonal [SB62a] Anti-Rabbit IgG light chain (HRP) (ab99697)
    Catalase was immunoprecipitated using 0.5mg Hela whole cell extract, 5µg of Rabbit polyclonal to Catalase (ab1877) and 50µl of protein G magnetic beads (lane 1). The antibody was incubated with the Protein G beads for 10min under agitation. No antibody was added to the control (lane 2). Hela whole cell extract diluted in RIPA buffer was added to each sample and incubated for 10min under agitation. Proteins were eluted by addition of 40µl SDS loading buffer and incubated for 10min at 70oC; 10µl of each sample was separated on a SDS PAGE gel, transferred to a nitrocellulose membrane, blocked with 5% BSA and probed with ab1877. Secodary: Mouse monoclonal [SB62a] Secondary Antibody to Rabbit IgG light chain (HRP) (ab99697). Bands: 60kDa: Catalase
  • Immunoprecipitation - Mouse monoclonal [SB62a] Anti-Rabbit IgG light chain (HRP) (ab99697)
    Immunoprecipitation - Mouse monoclonal [SB62a] Anti-Rabbit IgG light chain (HRP) (ab99697)
    Rad21 was immunoprecipitated using 0.5mg Hela whole cell extract, 5ug of Rabbit polyclonal to Rad21and 50µl of protein G magnetic beads (lane 1). The antibody was incubated with the Protein G beads for 10min under agitation. No antibody was added to the control (lane 2). Hela whole cell extractdiluted in RIPA buffer was added to each sample and incubated for 10min under agitation. Proteins were eluted by addition of 40µl SDS loading buffer and incubated for 10min at 70oC; 10µl of each sample was separated on a SDS PAGE gel, transferred to a nitrocellulose membrane, blocked with 5% BSA and probed with ab42478. Secondary: Mouse monoclonal [SB62a] Secondary Antibody to Rabbit IgG light chain (HRP) (ab99697) .. Band: 100kDa: Rad21; Non specific - 50kDa: We are unsure as to the identity of this extra band. Although the predicted band size is 75kDa based on Swiss-prot data, a band of 120kDa has been previously observed. Mol Cell Biol. 2002 Dec;22(23):8267-77 PMID: 12417729. Th
  • Western blot - Mouse monoclonal [SB62a] Anti-Rabbit IgG light chain (HRP) (ab99697)
    Western blot - Mouse monoclonal [SB62a] Anti-Rabbit IgG light chain (HRP) (ab99697)
    Lane 1: Rabbit IgG loaded at 1ug/well
    ab99697 diluted to 1:2000

Protocols

To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.

Click here to view the general protocols

References (43)

Publishing research using ab99697? Please let us know so that we can cite the reference in this datasheet.

ab99697 has been referenced in 43 publications.

  • Ardenkjær-Larsen J  et al. Insulin-induced serine 22 phosphorylation of retinoid X receptor alpha is dispensable for adipogenesis in brown adipocytes. Adipocyte 9:142-152 (2020). PubMed: 32249683
  • Sun J  et al. microRNA-93, upregulated in serum of nasopharyngeal carcinoma patients, promotes tumor cell proliferation by targeting PDCD4. Exp Ther Med 19:2579-2587 (2020). PubMed: 32256737
  • Christensen NR  et al. A high-affinity, bivalent PDZ domain inhibitor complexes PICK1 to alleviate neuropathic pain. EMBO Mol Med 12:e11248 (2020). PubMed: 32352640
  • Li J  et al. Dynamic changes in cis-regulatory occupancy by Six1 and its cooperative interactions with distinct cofactors drive lineage-specific gene expression programs during progressive differentiation of the auditory sensory epithelium. Nucleic Acids Res 48:2880-2896 (2020). PubMed: 31956913
  • Manolova V  et al. Oral ferroportin inhibitor ameliorates ineffective erythropoiesis in a model of ß-thalassemia. J Clin Invest 130:491-506 (2019). PubMed: 31638596
View all Publications for this product

Customer reviews and Q&As

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Excellent alternative when heavy chain overlies protein of interest in immunoprecipitation

 Excellent
Abreviews
abreview image
Application
Immunoprecipitation
My protein of interest is slightly larger than heavy chain making the use of usual (H+L) secondaries difficult for WB following immunoprecipitation. The two images exemplify the problem. The first is using a secondary that detects both heavy and light chain. Heavy chain band covers my protein of interest. The second image was obtained after stripping the membrane and repeating the WB, this time using ab99697. Now the heavy chain band in the IP lane has disappeared and is faintly existent from the previous experiment in the IgG lane.

Good sensitivity as well. This example is 1:5000, but now I am using 1:10,000.

Excellent!

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Verified customer

Submitted Jul 17 2014

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