Labshake search
Citations for Pall :
151 - 173 of 173 citations for Recombinant Human GTF2B Protein since 2019
Citations are collected from bioRxiv only, the total number of publications could be much larger.
-
bioRxiv - Cancer Biology 2023Quote: ... The proteins extracted from the sEVs were clean-up and concentrated using a 10 kDa Omega filtration centrifuge tubes (PALL, Nanosep), reduced ...
-
bioRxiv - Cancer Biology 2023Quote: Binding affinity of Arc protein to mRNA was measured using a bio-layer interferometer BLItz Pro (ForteBio, Pall Life Sciences, NY). Biotinylated mRNAs (Supplementary Methods) ...
-
bioRxiv - Cell Biology 2021Quote: ... Fifty microliter of supernatant was saved for protein assay (BCA assay, Pierce) while the rest was filtered (Pall Nanosep® OD003C33 centrifugal device with 3K Omega membrane, Pall Corp.) to remove molecules larger than 3,000 Daltons ...
-
bioRxiv - Biochemistry 2022Quote: ... Proteins were resolved by SDS–PAGE and either stained with Coomassie blue G250 or transferred to a nitrocellulose membrane (PALL, P-N66485) for protein immunoblotting using anti-phosphothreonine (Abcam ...
-
bioRxiv - Biochemistry 2022Quote: ... Proteins were resolved by SDS–PAGE and either stained with Coomassie blue G250 or transferred to a nitrocellulose membrane (PALL, P-N66485) for protein immunoblotting using anti-phosphothreonine (Abcam ...
-
bioRxiv - Molecular Biology 2021Quote: ... gels can also be processed for western blotting in which case transfer of proteins was setup onto a PVDF membrane (PALL Life Sciences). Transfer was carried out at 30V in appropriate transfer buffer for overnight ...
-
bioRxiv - Immunology 2021Quote: rS protein receptor binding kinetics was determined by bio-layer interferometry (BLI) using an Octet QK384 system (Pall Forté Bio, Fremont, CA). His-tagged human ACE2 (2 μg mL-1 ...
-
bioRxiv - Microbiology 2020Quote: S-protein receptor binding kinetics was determined by bio-layer interferometry (BLI) using an Octet QK384 system (Pall Forté Bio, Fremont, CA). Hist-tagged human ACE2 (2 μg mL−1 ...
-
bioRxiv - Biochemistry 2024Quote: ... The gel was equilibrated with blotting buffer for 10 min and the proteins were blotted onto a PVDF membrane (FluoroTrans W Membrane, PALL Life Science) via semidry blotting at 2 mA cm−2 for 1.5 h (Phos-tag gel ...
-
bioRxiv - Biochemistry 2022Quote: The binding of His-CaM to FR or FL-MLCK-FLAG protein in the presence of Ca2+ was analyzed using the Octet Red 96 (ForteBio, Pall Life Sciences) following the manufacturer’s procedures in duplicates ...
-
bioRxiv - Pathology 2024Quote: Lysate extracts (10-40 μg total protein) were separated on 4-20% or 10% Tris-glycine SDS-PAGE gels and transferred to nitrocellulose (Pall, Pensacola, FL) for probing with antisera as noted along with appropriate external controls ...
-
bioRxiv - Molecular Biology 2022Quote: ... Equivalent quantities of each protein sample were electrophoresed on SDS-PAGE gels and transferred to PVDF membranes (Pall Corporation, Ann Arbor, MI, USA). The primary antibodies directed against the following proteins were ...
-
bioRxiv - Cell Biology 2019Quote: ... The resolved proteins on the gels were transferred to PVDF membranes (FluoroTrans® W, 0.2 μm pore size, Pall Corporation, New York, USA) by semi-dry transfer at constant current ...
-
bioRxiv - Immunology 2020Quote: ... Protein from the gel was then transferred to a BioTrace Nitrocellulose transfer membrane with 0.2-μm pores (PALL laboratory; Port Washington, NY, USA). The membrane was blocked with 5% skim milk powder in tris-buffered saline (TBST) ...
-
bioRxiv - Molecular Biology 2024Quote: ... Proteins were separated by polyacrylamide gel electrophoresis (PAGE) and transferred to a BioTrace™ polyvinylidene fluoride membrane (Pall Corporation, New York, NY, USA) using a semi-dry blotting system (PEQLAB ...
-
bioRxiv - Biochemistry 2023Quote: A total of 100 μg of protein from each sample was loaded onto a 10 kDa filter device (Pall, Port Washington, NY, USA). After being washed two times with urea buffer (UA ...
-
bioRxiv - Biochemistry 2022Quote: ... One hundred micrograms of urine protein was added to the filter membrane of a 10 kDa ultrafiltration tube (Pall, Port Washington, NY, USA) using UA solution (8 mol/L urea ...
-
bioRxiv - Cell Biology 2021Quote: ... SDS-PAGE was performed with an equal amount (20 – 30 μg) of protein per lane and then were transferred onto a nitrocellulose membrane (PALL Life Sciences, Cat # 66485). Following transfer ...
-
bioRxiv - Cancer Biology 2019Quote: ... The process of enzymatic cleavage was performed as described previously [28]: the protein was loaded onto a 10 kDa filter (Pall, Port Washington, NY, USA); the urinary proteins were washed sequentially with UA (8 mol/L urea plus 0.1 mol/L Tris-HCl ...
-
bioRxiv - Biochemistry 2022Quote: ... One hundred micrograms of urinary proteins from each sample was added to the filter membrane of a 10 kDa ultrafiltration tube (Pall, Port Washington, NY, USA), which was placed in a 1.5 mL centrifuge tube ...
-
bioRxiv - Biochemistry 2024Quote: Uroprotein digestion: 100 μg of urinary protein sample was added to the membrane of a 10 kDa ultrafiltration tube (Pall, Port Washington, NY, USA), placed in an EP tube ...
-
bioRxiv - Molecular Biology 2019Quote: ... Equal amount of protein samples (∼30-50 μg) were resolved by SDS-PAGE and transferred to either an activated PVDF (polyvinylidene difluoride; Pall Life Sciences, New York, USA) or a nitrocellulose membrane (Pall Life Sciences ...
-
bioRxiv - Molecular Biology 2021Quote: ... The eluted proteins were separated by SDS-polyacrylamide gel electrophoresis (PAGE) and transferred to polyvinylidene fluoride (PVDF) membranes (Cat. #BSP0161; Pall Corporation, New York, NY, USA). The membranes were blocked with 5% non-fat milk and incubated with the following antibodies ...