Anti-IL17RB Neutralizing Antibody (V3S-0522-YC2362) (CAT#: V3S-0522-YC2362)

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  • fig1
    Figure 1 Mouse Anti-IL17RB Monoclonal Antibody (V3S-0522-YC2362) in DB
  • fig1
    Figure 2 Mouse Anti-IL17RB Monoclonal Antibody (V3S-0522-YC2362) in WB
  • fig1
    Figure 3 Mouse Anti-IL17RB Monoclonal Antibody (V3S-0522-YC2362) in ELISA
  • fig1
    Figure 4 Mouse Anti-IL17RB Monoclonal Antibody (V3S-0522-YC2362) Fab Fragment in DB
  • fig1
    Figure 5 Mouse Anti-IL17RB Monoclonal Antibody (V3S-0522-YC2362) Fab Fragment in WB
  • fig1
    Figure 6 Mouse Anti-IL17RB Monoclonal Antibody (V3S-0522-YC2362) Fab Fragment in ELISA

Datasheet

MSDS

COA

Summary
Property
Applications
Protocols
Target

Summary

Description This product is a monoclonal antibody derived from Mouse (Mus musculus), which can specifically recognize Interleukin 17 Receptor B. The antibody is expressed with mammalian cell transient expression system, serum-free and purified by affinity chromatography. The purity and integrity are tested via SDS-PAGE and SEC-HPLC analysis. Given an antigen, additional QC measures are also desired such as affinity testing and binding validation.
Specifically, the antibody is provided in multiple formats for in vivo and in vitro assays. The Invivo version features greater than 95% purity, ultra-low endotoxin levels (<1 EU/mg or 0.1 EU/mg), and is preservative, stabilizer, and carrier protein-free.
Clonality Monoclonal
Host Species Mouse
Target Species Human, Mouse
Isotype IgG

Property

Expression Species HEK293F or CHO
Conjugation None
Purity >95%, determined by SDS-PAGE and/or SEC-HPLC
Endotoxin <1 EU/mg, determined by LAL method
Purification Protein A affinity purified
Sterility 0.2 μM filtered
Formulation PBS, pH 7.4
Preservation No preservatives
Stabilizer No stabilizers
Storage Store at 4⁰C within a week. For longer storage, aliquot and store at -20⁰C.

Applications

Application WB; DB; ELISA; FC; Inhib; FuncS
Application Notes The antibody is recommended for detection of IL17RB by ELISA, FC, Inhib, FuncS assays.

Protocols

ELISA Enzyme-Linked Immunosorbent Assay Protocol
WB Western Blot Protocol
FC Flow Cytometry Protocol

Target

Target IL17RB
Alternative Name Interleukin 17 Receptor B
Gene ID 55540
UniProt Q9NRM6
Research Area Immunology
Related Disease Asthma, Ulcerative colitis and Crohn's disease

Tested Data

DB

Figure 1 Mouse Anti-IL17RB Monoclonal Antibody (V3S-0522-YC2362) in DB

Dot Blot analysis of V3S-0522-YC2362 was performed by coating with human IL17RB protein (His tag).
V3S-0522-YC2362 incubation concentration: 2 μg/mL.
HRP conjugated Anti-Mouse IgG as a secondary antibody (1: 2000)

Figure 1 Mouse Anti-IL17RB Monoclonal Antibody (V3S-0522-YC2362) in DB

WB

Figure 2 Mouse Anti-IL17RB Monoclonal Antibody (V3S-0522-YC2362) in WB

Western blot analysis of V3S-0522-YC2362 was performed by loading human IL17RB protein (His tag) onto a 12% Tris-HCl polyacrylamide gel. Proteins were transferred to a CN membrane and blocked with 5% skim milk for at least one hour. Membranes were probed with V3S-0522-YC2362 and HRP conjugated Anti-Mouse IgG as a secondary antibody (1: 2000). Chemiluminescent detection was performed.

Lane 1: Reduced antigen (0.1 μg)
Lane 2: Reduced antigen (0.3 μg)
Lane 3: Reduced antigen (0.6 μg)

Figure 2 Mouse Anti-IL17RB Monoclonal Antibody (V3S-0522-YC2362) in WB

ELISA

Figure 3 Mouse Anti-IL17RB Monoclonal Antibody (V3S-0522-YC2362) in ELISA

ELISA analysis of V3S-0522-YC2362 was performed by coating with human IL17RB protein (His tag). Then blocked with BSA and incubated with V3S-0522-YC2362. The HRP conjugated Anti-Mouse IgG as a secondary antibody (1: 2000). Detection was performed using TMB substrate and stopped with sulfuric acid. The absorbances were read on a spectrophotometer at 450 nm.

Figure 3 Mouse Anti-IL17RB Monoclonal Antibody (V3S-0522-YC2362) in ELISA

DB

Figure 4 Mouse Anti-IL17RB Monoclonal Antibody (V3S-0522-YC2362) Fab Fragment in DB

Dot Blot analysis of V3S-0522-YC2362 Fab fragment was performed by coating with human IL17RB protein (His tag).
V3S-0522-YC2362-F(E) incubation concentration: 2 μg/mL.
HRP conjugated Anti-His tag as a secondary antibody (1: 2000)

Figure 4 Mouse Anti-IL17RB Monoclonal Antibody (V3S-0522-YC2362) Fab Fragment in DB

WB

Figure 5 Mouse Anti-IL17RB Monoclonal Antibody (V3S-0522-YC2362) Fab Fragment in WB

Western blot analysis of V3S-0522-YC2362 Fab fragment was performed by loading human IL17RB protein (His tag) onto a 12% Tris-HCl polyacrylamide gel. Proteins were transferred to a CN membrane and blocked with 5% skim milk for at least one hour. Membranes were probed with V3S-0522-YC2362-F(E) and HRP conjugated Anti-His tag as a secondary antibody (1: 2000). Chemiluminescent detection was performed.

Lane 1: Reduced antigen (0.1 μg)
Lane 2: Reduced antigen (0.3 μg)
Lane 3: Reduced antigen (0.6 μg)

Figure 5 Mouse Anti-IL17RB Monoclonal Antibody (V3S-0522-YC2362) Fab Fragment in WB

ELISA

Figure 6 Mouse Anti-IL17RB Monoclonal Antibody (V3S-0522-YC2362) Fab Fragment in ELISA

ELISA analysis of V3S-0522-YC2362 Fab fragment was performed by coating with human IL17RB protein (His tag). Then blocked with BSA and incubated with V3S-0522-YC2362-F(E). The HRP conjugated Anti-His tag as a secondary antibody (1: 2000). Detection was performed using TMB substrate and stopped with sulfuric acid. The absorbances were read on a spectrophotometer at 450 nm.

Figure 6 Mouse Anti-IL17RB Monoclonal Antibody (V3S-0522-YC2362) Fab Fragment in ELISA

For research use only, not directly for clinical use.
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