Rabbit IgG kappa Light Chain Mouse Monoclonal Antibody [1-14]
cat.: M0809-1
Product Type: Mouse monoclonal IgG1, primary antibodies
Species reactivity: Rabbit
Applications: WB, ELISA, IP
Clonality: Monoclonal
Clone number: 1-14
Form: Liquid
Storage condition: Shipped at 4℃. Store at +4℃ short term (1-2 weeks). Store at -20℃ long term.
Storage buffer: 1*PBS (pH7.4), 0.2% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 2ug/ul
Purification: Immunogen affinity purified.
Molecular weight: 25 kDa
Isotype: IgG1
Immunogen: Purified Rabbit IgG κ Light Chain.
Positive control: Rabbit IgG
Subcellular location: serum/plasma
Recommended Dilutions:
  IP
  WB
  ELISA

1:500-1,000
1:500-1,000
1:1,000-2,000
Alternative names: IgG κ IgGκ
Images
M0809-1_1.jpg Fig1: Western blot analysis of Rabbit IgG kappa Light Chain on different lysates with Rabbit anti-Rabbit IgG kappa Light Chain antibody (M0809-1) at 1/1,000 dilution.

Lane 1: Rabbit IgG lysate
Lane 2: Mouse IgG lysate
Lane 3: Human IgG lysate

Lysates/proteins at 10 ng/Lane.
Exposure time: 30 seconds; ECL: K1801

Blocking: 5% NFDM/TBST, 1 hour at room temperature
Primary antibody: M0809-1, 1/1,000 in 5% NFDM/TBST, overnight at 4 ℃
Secondary antibody: Goat Anti-Mouse IgG-HRP (HA1006), 1/50,000 in 5% NFDM/TBST, 1 hour at room temperature

Predicted band size: 25 kDa
Observed band size: 25 kDa
M0809-1_2.jpg Fig2: Indirect ELISA analysis of Rabbit IgG kappa Light Chain was performed by coating wells of a 96-well plate with 50 µL per well of Rabbit IgG / Mouse IgG / Human IgG diluted in carbonate/bicarbonate buffer, at a concentration of 1 µg/mL overnight at 4℃. Wells of the plate were washed, blocked with 1%BSA blocking buffer for 1 hour at 37℃, and incubated with 50 µL per well of Rabbit IgG kappa Light Chain monoclonal antibody serial diluted starting from a concentration of 1µg/mL for 45 minutes at 37℃. The plate was washed and incubated with 50 µL per well of an HRP-conjugated goat anti-mouse IgG secondary antibody at a dilution of 1/80,000 for 30 minutes at 37℃. Detection was performed using an Ultra TMB Substrate for 10 minutes at 37℃ in the dark. The reaction was stopped with sulfuric acid and absorbances were read on a spectrophotometer at 450 nm.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.