Rat IgG (H+L chain) F(ab')2 Fragment Donkey Polyclonal Antibody

CAT#: R1428R

Rat IgG (H+L chain) F(ab')2 Fragment donkey polyclonal antibody, PE

Specifications

Product Data

• Recommended Dilution: Suitable for Immunomicroscopy (1:100-1:200) and Flow Cytometry (1:100-1:200) or FACS analysis as well as other antibody based fluorescent assays requiring extremely low background levels, absence of F(c) mediated binding, lot-to-lot consistency, high titer and specificity.
• Host: Donkey
• Clonality: Polyclonal
• Immunogen: Rat IgG whole molecule
• Specificity: This product was prepared from monospecific antiserum by Immunoaffinity chromatography using Rat IgG coupled to agarose beads followed by solid phase adsorption(s) to remove any unwanted reactivities, pepsin digestion and chromatographic separation.
  Assay by Immunoelectrophoresis resulted in a single precipitin arc against anti-Phycoerythrin, anti-Donkey Serum, Rat IgG and Rat Serum.
  No reaction was observed against anti-Pepsin, anti-Donkey IgG F(c), Bovine, Chicken, Goat, Guinea Pig, Syrian Hamster, Horse, Human, Mouse, Rabbit or Sheep Serum Proteins.
• Formulation: 0.02 M Potassium Phosphate, 0.15 M Sodium Chloride; pH 7.2 with 0.01% (w/v) Sodium Azide as preservative and 10 mg/ml Bovine Serum Albumin (BSA), IgG and Protease free, as stabilizer.
  Label: PE
  State: Lyophilized F(ab')2 fragments.
  Label: R-Phycoerythrin ( isolated from a culture of red algae. Subunit structure - (αβ)6γ Apparent Molecular Weight - 240 kDa (alpha 20 kDa, beta 20 kDa, gamma 30 kDa). Phycobiliprotein Concentration: 0.5 mg/ml (determined by absorbance = 82.0 at 565 nm for a 1% solution for only those molecules to which at least one molecule of active antibody is bound)
  Absorption emission: 490 nm, 545 nm and 565 nm / 580 nm
• Reconstitution Method: Restore with 1.0 ml of deionized water (or equivalent).
• Purification: Immunoaffinity chromatography.
• Conjugation: PE
• Storage: Store the antibody (undiluted) at 2-8°C prior to opening.
  DO NOT FREEZE!
  Store reagent in the dark. Use subdued lighting during handling and incubation
  of cells prior to analysis.
  Dilute only prior to immediate use.