Recombinant Anti-ERBB2 Antibody (V3S-0822-YC3125) (CAT#: V3S-0822-YC3125)

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  • fig1
    Figure 1 Anti-ERBB2 Monoclonal Antibody (V3S-0822-YC3125) in ELISA
  • fig1
    Figure 2 Anti-ERBB2 Monoclonal Antibody (V3S-0822-YC3125) in WB
  • fig1
    Figure 3 Anti-ERBB2 Monoclonal Antibody (V3S-0822-YC3125) in SDS-PAGE

Datasheet

MSDS

COA

Summary
Property
Applications
Protocols
Target

Summary

Description This product is a mouse monoclonal antibody provided by Creative Biolabs. The antibody is capable of recognizing human erb-b2 receptor tyrosine kinase 2 (ERBB2). It can be used for ERBB2 detection in Enzyme-Linked Immunosorbent Assay (ELISA), Flow Cytometry (FC). The antibody is expressed in mammalian cells (293F or CHO) with antibody encoding genes and purified by affinity chromatography. Each lot of this antibody is quality control tested by SDS-PAGE and SEC-HPLC analysis. For highly sensitive assays, we recommend the ultra purified form of the product, which has a lower endotoxin limit than standard antibody, less than 1 EU/mg or even 0.1 EU/mg.
Clonality Monoclonal
Host Species Mouse
Target Species Human
Isotype IgG2a kappa

Property

Expression Species HEK293F or CHO cell line
Conjugation Unconjugated, also available for Biotin, HRP, FITC and PE-labeled form.
Purity >95%, determined by SDS-PAGE and SEC-HPLC
Endotoxin <1 EU/mg, determined by LAL method
Purification Protein A or G purified
Sterility 0.2 μM filtered
Formulation PBS, pH 7.4
Preservation No preservatives
Storage Store at 4°C within one or two weeks. Store at -20°C for long term. Avoid repeated freeze/thaw cycles. Refer to the COA file for specifics.

Applications

Application WB; ELISA; FC

Protocols

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

Target

Target ERBB2
Alternative Name NEU; NGL; HER2; TKR1; CD340; HER-2; MLN 19; HER-2/neu
Gene ID 2064
UniProt P04626
Research Area Cancer Research

Tested Data

ELISA

Figure 1 Anti-ERBB2 Monoclonal Antibody (V3S-0822-YC3125) in ELISA

ELISA analysis of V3S-0822-YC3125 was performed by coating with Recombinant Human ERBB2 Protein. Then blocked with BSA, and incubated with Anti-Human ERBB2 Antibody (V3S-0822-YC3125). The HRP-conjugated goat anti-mouse IgG as a secondary antibody. Detection was performed using TMB substrate and stopped with sulfuric acid. The absorbances were read on a spectrophotometer at 450 nm.

Figure 1 Anti-ERBB2 Monoclonal Antibody (V3S-0822-YC3125) in ELISA

WB

Figure 2 Anti-ERBB2 Monoclonal Antibody (V3S-0822-YC3125) in WB

Western blot analysis of V3S-0822-YC3125 was performed by loading Recombinant Human ERBB2 Protein (lane 1, Non-Reducing Antigen, 0.2μg; lane 2, Reducing Antigen, 0.2μg) 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-0822-YC3125 and HRP Goat Anti-Mouse IgG as a secondary antibody. Chemiluminescent detection was performed.

Figure 2 Anti-ERBB2 Monoclonal Antibody (V3S-0822-YC3125) in WB

SDS-PAGE

Figure 3 Anti-ERBB2 Monoclonal Antibody (V3S-0822-YC3125) in SDS-PAGE

SDS-PAGE analysis of V3S-0822-YC3125 in non-reduced and β-mercaptoethanol-reduced conditions. Gel stained for 30 minutes with Coomassie Blue. As a result of different β-mercaptoethanol-reduced proteins (Heavy chain and Light chain) migrate as about 50 kDa and 25 kDa, respectively. And non-reduced protein migrates as 130-180 kDa.

Figure 3 Anti-ERBB2 Monoclonal Antibody (V3S-0822-YC3125) in SDS-PAGE

For research use only, not directly for clinical use.
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