Bovine IgG Bovine Protein
Specifications
| Product Data | |
| Species | Bovine |
|---|---|
| Protein Source | Serum |
| Concentration | 1.0 mg/mL by UV absorbance at 280 nm |
| Purity | This product was prepared from normal serum by delipidation, salt fractionation, ion exchange chromatography followed by conjugation and extensive dialysis against the buffer stated above. Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-Bovine IgG, anti-Bovine Serum and anti-Alkaline Phosphatase (calf intestine). |
| Buffer | 0.05 M Tris Chloride, 0.15M Sodium Chloride, 0.001M Magnesium Chloride, 0.0001M Zinc Chloride, 50% (v/v) Glycerol; pH 8.0 |
| Preparation | Liquid |
| Protein Description | Bovine IgG |
| Note | Bovine IgG whole molecule alkaline phosphatase conjugation can be utilized as a control or standard reagent in Western Blotting and ELISA experiments. |
| Storage | Store vial at 4° C before opening. DO NOT FREEZE. This product is stable at 4° C as an undiluted liquid. Dilute only prior to immediate use. Freezing alkaline phosphatase conjugates will result in a substantial loss of enzymatic activity. |
| Stability | Expiration date is one (1) year from date of receipt. |
| Shipping | Blue Ice |
| Reference Data | |
| Synonyms | Bovine IgG Alkaline Phosphatase conjugation, Bovine IgG alk phos conjugation, Alkaline phosphatase conjugated Bovine IgG, alk phos conjugated Bovine IgG |
| Summary | Secreted as part of the adaptive immune response by plasma B cells, immunoglobulin G constitutes 75% of serum immunoglobulins. Immunoglobulin G binds to viruses, bacteria, as well as fungi and facilitates their destruction or neutralization via agglutination (and thereby immobilizing them), activation of the compliment cascade, and opsonization for phagocytosis. The whole IgG molecule possesses both the F(c) region, recognized by high-affinity Fc receptor proteins, as well as the F(ab) region possessing the epitope-recognition site. Both heavy and light chains of the antibody molecule are present. |
Reviews
Documents
| FAQs |
| SDS |
Resources
| Recombinant Protein Resources |
Citations
Neuraminidase-associated plasminogen recruitment enables systemic spread of natural avian Influenza viruses H3N1
Schön, Breithaupt, Höper et al
PLoS Pathog (2021) 17 (4), e1009490 DOI: 10.1371/journal.ppat.1009490
Schön, Breithaupt, Höper et al
PLoS Pathog (2021) 17 (4), e1009490 DOI: 10.1371/journal.ppat.1009490
Cited by 13
AI Summary: OriGene’s goat-anti-chicken-IgY-FITC secondary antibody was used to detect chicken antibodies in cell-based immunofluorescence assays, enabling visualization of viral antigen-antibody interactions in the study.
Snippet: r 1 hour of incubation we washed the cells three times with washing buffer (0,025% Tween-20/PBS), before adding the fluorescein isothiocyanate (FITC) labeled secondary Ab (goat-anti-chicken-IgY-FITC (OriGene Technologies GmbH, Maryland, USA)), diluted 1:400 in blocking buffer. Following 1-hour incubation, the cells were washed three times with washing buffer and finally 20% glycerol in PBS was add...
Showing 1-1 of 1 papers.
Powered by BizGenius
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen
complexities in the preparation of your product. International customers may expect an additional 1-2 weeks
in shipping.
Related Products
- Price:
- Actual Price:
Welcome to OriGene AI!
I'm your AI-powered guide to everything OriGene.
Ask me anything:
- Product specs
- Ordering help
- Technical questions
- How to find exactly what your experiment needs
Prefer a live agent? Connect with us by clicking the green chat icon, as seen in the image below or email our team at custsupport@origene.com.
