Biotin Conjugated Mouse IL-17E/IL-25 Recombinant Rabbit Monoclonal Antibody [PSH15-34]
cat.: HA725045B
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Mouse
Applications: ELISA(Det), ELISA
Clonality: Monoclonal
Clone number: PSH15-34
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), 0.1% BSA, 40% Glycerol, 0.05% Proclean 300.
Concentration: 1ug/ul
Purification: Protein A affinity purified.
Isotype: IgG
Immunogen: Recombinant protein within Mouse IL-17E/IL-25 aa 17-169 (HA211130).
Positive control: Recombinant Mouse IL-17E/IL-25 protein (HA211130).
Subcellular location: Secreted.
Recommended Dilutions:
  ELISA(Det)
  ELISA

Use at an assay dependent concentration. Can be paired for Sandwich ELISA with Rabbit monoclonal [PSH15-26] to Mouse IL-17E/IL-25 antibody (Capture) (HA725043) and Recombinant Mouse IL-17E/IL-25 protein (HA211130) as the standard. The reference range value is 78.1-10,000 pg/mL.
Use at an assay dependent concentration.
Uniprot #: SwissProt: Q8VHH8 Mouse
Alternative names: IL 17E IL 25 IL-17E IL-25 IL17e IL25 IL25_HUMAN Interleukin 17E Interleukin 25 Interleukin-17E Interleukin-25 Interleukin17E Interleukin25 OTTHUMP00000027946 OTTHUMP00000246238 UNQ3120/PRO10272
Images
HA725045B_1.png Fig1: Sandwich ELISA analysis of Mouse IL-17E/IL-25 matched pair antibodies

Capture: HA725043, Mouse IL-17E/IL-25 Rabbit mAb [PSH15-33]
Detector: HA725044, Mouse IL-17E/IL-25 Rabbit mAb [PSH15-34]

Elisa assay was performed by coating wells of a 96-well plate with 100 µl per well of capture antibody (HA725043) diluted in carbonate/bicarbonate buffer, at a concentration of 2 µg/mL overnight at 4℃. Wells of the plate were washed, blocked with 150 µl 0.05% tween-20 1% BSA blocking buffer, and incubated with serial diluted Recombinant Mouse IL-17E/IL-25 protein (HA211130) starting from 10,000 pg/ml to 0 pg/ml and detect antibody (HA725044, Biotin, 0.2 µg/ml) for 1 hour at 30℃ with shaking. Then the plate was washed and incubated with 100 µl per well of SA-HRP for 0.5 hour at 30℃ with shaking. Detection was performed using an Ultra TMB Substrate for 10 minutes at room temperature 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”.