The largest database of trusted experimental protocols

Antibody against mt

Manufactured by Agilent Technologies

The Antibody against MT is a laboratory reagent used to detect and quantify the presence of microtubules (MT) in biological samples. This antibody specifically binds to and recognizes microtubules, which are cytoskeletal structures found in eukaryotic cells. The core function of this product is to provide a reliable tool for researchers to study the dynamics and organization of the microtubule network in various cell types and experimental conditions.

Automatically generated - may contain errors

2 protocols using antibody against mt

1

Modified Western Blot Protocol for Protein Expression

Check if the same lab product or an alternative is used in the 5 most similar protocols
MT expression was detected using a modified western blot protocol, as previously described [20 (link)], using antibody against MT (Dako, 1:500 dilution). A regular western blot protocol was performed as described in our previous studies [11 (link), 21 (link)]. Primary antibodies used included TGF-β1 (Cell Signaling, 1:500 dilution), connective tissue growth factor (CTGF, Santa Cruz Biotechnology, 1:500 dilution), plasminogen activator inhibitor-1 (PAI-1, BD Biosciences, San Jose, CA, 1:1,000 dilution), VCAM-1(Santa Cruz Biotechnology, 1:1000 dilution), 3-NT (Millipore, 1:1000 dilution), 4-hydroxy-2-nonenal (4-HNE, Alpha Diagnostic Int., San Antonio, TX, 1:3000 dilution), Nrf2 (Santa Cruz Biotechnology, 1:1000 dilution), Keap1 (Santa Cruz Biotechnology, 1:500 dilution), Histone H3 (H3, Santa Cruz Biotechnology, Dallas, TX, 1:500 dilution), and β-actin (Actin, Santa Cruz Biotechnology, 1:2000 dilution). Appropriate secondary antibodies (Santa Cruz Biotechnology) were used.
+ Open protocol
+ Expand
2

Cardiac Tissue Protein Expression Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Cardiac tissue was homogenized with RIPA lysis buffer to prepare the lysate. Protein samples were subjected to SDS‐PAGE and then transferred to PVDF membranes (Bio‐Rad, Hercules, CA). After blocking with 5% BSA (Bovine serum albumin), the membrane was incubated with the antibody. The primary antibodies used include Fibronectin (FN), TGF‐β, ICAM‐1, VCAM‐1, IL‐1β, all of which were purchased from Abcam, Cambridge, MA. Phospho (p)‐t‐Akt, total (t‐)Akt, p‐Akt1, Akt1, p‐Akt2, Akt2, pGSK‐3β, GSK‐3β, p‐GS, GS, pAS160, AS160, pERK1/2, ERK1/2, hexokinase II (HK II), all of which were purchased from Cell Signaling Technology, Beverly, MA. COL1A1, β‐Actin, all of which were purchased from Santa Cruz Biotech. Inc 3‐NT was purchased from Millipore. 4‐HNE was purchased from Alpha Diagnostic. Inc pPFKFB2, PFKFB2 and glycogen phosphorylase (GP) were purchased from Thermo Fisher Scientific, Waltham, MA. Antibody against MT was purchased from DakoCytomation, Santa Clara, CA. The ratios of total protein of Akt2, t‐Akt, Akt1, GSK‐3β, GS, AS160, PFKFB2 and ERK1/2 to β‐Actin are in the supplementary figures.
+ 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!