General Western Blot Reagents
Cell Signaling Technology Mouse Brain Tissue Control Extracts 100 ul
Mouse Brain Tissue Control Extracts 100 ul
American Research Products Inc Mouse Cytochrome P450 2E1 CYP
Mouse Cytochrome P450 2E1 (CYP2E1) ELISA kit from CUSABIO Detection Range 39 pg/mL-2500 pg/mL Sensitivity 9 75 pg/mL Sample serum plasma tissue homogenates cell lysates Method Sandwich
Cosmo Bio Usa Inc SOLUTION CAN GET SIGNAL 250ML
Antibody signal enhancer solution set for 1 antibody (250ml). Simply dilute Ab to improve sensitivity, background, S/N ratio in most applications. Saves ab. Saves valuable antibody. (Solution 1 only)
Cell Signaling Technology p44/42 MAPK (Erk1/2) Control Cell Extracts 150 µl
p44/42 MAPK (Erk1/2) Control Cell Extracts 150 µl
Bioworld Re-Probe Solution western Blots, 125 mL
Re-Probe Solution, Western BlotsRe-Probe is supplied as 5X. The 125ml kit sufficient for 25 blots. Not recommended for chromogenic substrates.
American Research Products Inc Rat Cytochrome P450 19A1 CYP1
Rat Cytochrome P450 19A1 (CYP19A1) ELISA kit from CUSABIO Detection Range 18 75 pg/mL-1200 pg/mL Sensitivity 4 68 pg/mL Sample serum plasma tissue homogenates Method Sandwich
ABclonal Technology Cytochrome P450 2E1 CYP2E1
This gene encodes a member of the cytochrome P450 superfamily of enzymes The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol steroids and other lipids This protein localizes to the endoplasmic reticulum and is induced by ethanol the diabetic state and starvation The enzyme metabolizes both endogenous substrates such as ethanol acetone and acetal as well as exogenous substrates including benzene carbon tetrachloride ethylene glycol and nitrosamines which are premutagens found in cigarette smoke Due to its many substrates this enzyme may be involved in such varied processes as gluconeogenesis hepatic cirrhosis diabetes and cancer
Bioworld Blot Stripping Buffer II (4X), 250 mL
Product DescriptionBlot stripping buffer II (4x) contains enough liquid concentrate to make 4L of 1X solution. Product is 0.2M glycine and has a pH value of 2.5.To use this product, place the membrane into stripping buffer for 30-45 minutes with gentle agitation. Buffer should be heated to approximately 50°C for incubation. Wash membrane 3 times with TBST or PBST before reprobing.Product is ultra pure grade.
Sigma Aldrich Fine Chemicals Biosciences PVDf Western Blotting Memb
PVDf Western Blotting Membranes are hydrophobic microporous polyvinylidene difluoride (PVDf) membranes with a pore size of 0.2mum. The PVDf Western Blotting Membranes are ideal for western and dot blots. The high binding capacity high mechanical strength and chemical resistance of the PVDf membrane makes it specifically useful for protein blotting. The combination of strong sample retention and low background binding generates excellent signal-to-noise ratios in colorimetric and chemiluminescent detection. The primary binding mechanism includes electrostatic and hydrophobic nature. Adsorption Goat IgG 294mug/cm2 BSA 131mug/cm2 insulin 85mug/cm2
Seracare Life Sciences Inc LUMIGLO HRP CHEMI SUBS
Non-isotopic, luminol-based chemiluminescent substrate designed for the rapid and sensitive detection of peroxidase labeled-conjugates. It provides increased sensitivity over chromogenic substrates in both blotting and ELISA applications. In blotting applications, permanent results are recorded on X-ray film. The use of LumiGLO allows for multiple stripping and reprobing of blots. In ELISA, positive reactions are read and rapidly detected using a luminometer. LumiGLO provides a dynamic range that is linear for a longer period of time than other chemiluminescent substrates. 2-Component format, simply mix and use. Safe to use: non-hazardous.
LICORbio NewBlot™ PVDF Stripping Buffer for PVDF Membranes (100 mL)
NewBlot PVDF stripping buffer is specially formulated for IRDye secondary antibodies including IRDye 800CW, IRDye 680RD, and IRDye 680LT. NewBlot PVDF is intended for PVDF membranes only and is ideal for removal of secondary antibody.