7069881

Armenian Hamster IgG Isotype Control (eBio299Arm), Functional Grade, eBioscience™, Invitrogen™

Armenian Hamster Isotype Control

Manufacturer: Fischer Scientific

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Antigen

Armenian Hamster IgG

Concentration

1 mg/mL

Conjugate

Functional Grade

Host Species

Armenian Hamster

Target Species

Not Applicable

Gene Alias

IgG; Immunoglobulin G; ImmunoglobulinG

Primary or Secondary

Isotype Control (Primary)

Content And Storage

4° C

Clone

eBio299Arm

Applications

Control, Flow Cytometry, Functional Assay

Form

Liquid

Regulatory Status

RUO

Formulation

PBS with no preservative; pH 7.2

Isotype

IgG

Purification Method

Affinity chromatography

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Description

  • Description: The eBio299Arm monoclonal antibody is useful as an isotype control immunoglobulin
  • Applications Reported: The eBio299Arm antibody has been reported for use as an isotype control for flow cytometry
  • Applications Tested: This eBio299Arm antibody has been tested by LAL assay to determine endotoxin level and by immunofluorescent staining and flow cytometric analysis of mouse splenocytes and normal human peripheral blood
  • Storage and handling: Use in a sterile environment
  • Filtration: 0.2 μm post-manufacturing filtered
  • Purity: Greater than 90%, as determined by SDS-PAGE
  • Endotoxin Level: Less than 0.001 ng/μg antibody, as determined by LAL assay
  • Aggregation: Less than 10%, as determined by HPLC
  • The isotype of a primary antibody and the application it is being used in can result in background staining
  • Primary antibody background noise can be caused by binding to Fc receptors on target cells; by non-specific interactions with cellular proteins, carbohydrates, and lipids; or by cell autofluorescence
  • Isotype control antibodies can act as negative controls to help differentiate non-specific background signal from specific antibody signal because they have no relevant specificity to a target antigen
  • While isotype controls are most commonly used in flow cytometry, they are useful in other applications such as chromatin immunoprecipitation (ChIP), immunohistochemistry, and gel shifts
  • Isotype controls should match with the primary antibody species and isotype so that the level of specific staining by the primary antibody may be accurately determined
  • If using directly labeled primary antibodies, the isotype control works best if conjugated with the same label as the test antibody.