The largest database of trusted experimental protocols

Goat antihuman fcγ

Manufactured by Jackson ImmunoResearch

Goat–antihuman Fcγ is a laboratory reagent used to detect and quantify human immunoglobulins. It is a polyclonal antibody produced in goats that specifically binds to the Fc region of human IgG antibodies. This reagent can be used in various immunoassays and other applications that require the detection or measurement of human IgG.

Automatically generated - may contain errors

2 protocols using goat antihuman fcγ

1

Recombinant Protein Purification and Characterization

Check if the same lab product or an alternative is used in the 5 most similar protocols
Standard laboratory chemicals were purchased from Carl Roth. Ham's F‐12 growth medium, fetal bovine serum, PBS, and glutamine were from Biochrom. Blasticidin S was obtained from InvivoGen. Hygromycin B came from Carl Roth. ProCHO4 growth medium was from Lonza. All enzymes for cloning were bought from New England Biolabs. Doxycycline hydrochloride, ADP sodium salt, and ATP disodium salt hydrate were purchased from Sigma‐Aldrich. Part of the recombinant hirudin was a kind gift from Prof. Christian P. Sommerhoff (University of Munich), and another part was purchased from Celgene. Collagen‐related peptide was synthesized at AnaSpec and chemically cross‐linked. DiOC6 (3,3′‐dihexyloxacarbocyanine iodide) was from Life Technologies. midazolam (Dormicum; Roche) was purchased from Roche, and medetomidine (Dormitor; Pfizer) and fentanyl were both from Janssen‐Cilag. Recombinant soluble human CD39 (solCD39) was obtained from R&D Systems. Goat–antihuman Fcγ and goat–antihuman IgG (H+L)‐POD (peroxidase) were purchased from Jackson ImmunoResearch.
+ Open protocol
+ Expand
2

Anti-CD20 Antibody Binding Assay

Check if the same lab product or an alternative is used in the 5 most similar protocols
Anti-hCD20 Abs diluted in DPBS/1% bovine serum albumin (BSA) were incubated with 6×105 Raji cells in V-bottom 96-well plates at 4°C for 1 hr in a final volume of 50 μL. The cells were washed with cold DPBS/1% BSA and incubated at 4°C for 1 hr with 50 μg/mL goat anti-human Fcγ (Jackson ImmunoResearch) labeled with Atto 488 (A488) NHS ester as previously described [27 (link)]. Binding of mAbs to live single cells gated by light scatter characteristics was measured using a BD LSRFortessa X-20 flow cytometer. Representative flow cytometry histograms are presented in Supplementary Figure S1. The binding of bacteriophage displaying the Fab portions of the chicken Abs to hCD20-transfected Chinese hamster ovary (CHO) cells was also measured (Supplementary Figure S2).
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!