The largest database of trusted experimental protocols

Donkey anti goat igg horseradish peroxidase hrp

Manufactured by Santa Cruz Biotechnology
Sourced in United States

Donkey anti-goat IgG–horseradish peroxidase (HRP) is a secondary antibody conjugate used in immunoassays and Western blotting applications. It is composed of donkey-derived antibodies that specifically recognize and bind to goat immunoglobulin G (IgG), coupled with the enzyme horseradish peroxidase (HRP).

Automatically generated - may contain errors

2 protocols using donkey anti goat igg horseradish peroxidase hrp

1

NF-κB Activation Assay in THP-1 and J774 Cells

Check if the same lab product or an alternative is used in the 5 most similar protocols
Unless stated otherwise all materials were obtained from Sigma Aldrich (Poole, Dorset, U.K.) in their highest purity. RPMI, Dulbecco's modified Eagle medium (DMEM), phosphate buffered saline (PBS), foetal calf serum (FCS), Glutamax, penicillin and streptomycin were obtained from Invitrogen (Paisley, U.K.). THP-1 and J774 cells were obtained from the European Collection of Animal Cell Cultures (Salisbury, Wiltshire, U.K.). [γ-32P]-ATP (370MBq/ml, 10 mCi/ml), polyvinylidene difluoride membrane (PVDF) and poly(dI–dC)–poly(dI–dC) was obtained from Amersham Biosciences (Little Chalfont, Buckinghamshire, U.K.). NF-κB Gel Shift Assay System was obtained from Promega (Southampton, Hampshire, U.K.). Goat polyclonal antibodies for p50 (cross reactive with p105), rabbit polyclonal antibodies to p50, p65 or IκBα and actin, donkey anti-goat IgG–horseradish peroxidase (HRP) and supershift antibodies were obtained from Santa Cruz Biotechnology (Santa Cruz, CA, U.S.A.). Donkey anti-goat IgG–fluorescein isothiocyanate (FITC) was obtained from AbD Serotec (Oxford, U.K.). Lymphoprep was obtained from Axis-Shield (Oslo, Norway).
+ Open protocol
+ Expand
2

Immunohistochemical Staining for Neurodegenerative Markers

Check if the same lab product or an alternative is used in the 5 most similar protocols
Immunohistochemical staining was performed according to a previously described method (Gu et al. 2015 (link)). The sections were reacted with specific primary antibodies for Aβ (1:300; Abcam, Inc., Cambridge, MA, USA), glial fibrillary acidic protein (GFAP) (1:300; Santa Cruz Biotechnology, Inc., Santa Cruz, CA, USA), ionize calcium-binding adapter molecule 1 (IBA-1) (1:300; Abcam, Inc., Cambridge, MA, USA), inducible nitric oxide synthase (iNOS) (1:300; Novus Biologicals, Inc., Littleton) and cyclooxygenase-2 (COX-2) (1:300; Cell Signaling Technology, Inc., Beverly, MA, USA). Tissues were then incubated with the corresponding conjugated secondary antibodies: goat anti-rabbit, goat anti-mouse, or donkey anti-goat IgG-horseradish peroxidase (HRP) (1:5000; Santa Cruz Biotechnology Inc. Santa Cruz, CA, USA). The sections were evaluated under a light microscope (Microscope Axio Imager.A2, Carl Zeiss, Oberkochen, Germany) (×50 or ×200 or ×400).
+ 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!