Journal: Cell reports

Article Title: G2 arrest primes hematopoietic stem cells for megakaryopoiesis

doi: 10.1016/j.celrep.2024.114388

Figure Lengend Snippet: KEY RESOURCES TABLE

Article Snippet: Fluorescent Mounting Media with DAPI , OriGene , E19-18.

Techniques: Recombinant, Adhesive, Purification, Blocking Assay, Amplification, Random Hexamer Labeling, Reverse Transcription, SYBR Green Assay, Sterility, Imaging, Software

Journal: Histopathology

Article Title: Sinonasal adenosquamous carcinomas arising in seromucinous hamartoma or respiratory epithelial adenomatoid hamartoma with atypical features: Report of five detailed clinicopathological and molecular characterisation of rare entity

doi: 10.1111/his.15369

Figure Lengend Snippet: Clinical data and follow‐up of five cases of adenosquamous carcinoma

Article Snippet: The following antibodies were used: p16 (R15A, rabbit monoclonal antibody, 1:100 dilution; DB Biotech, Kosice, Slovakia), CK7 (OV‐TL 12/30, 1:200 dilution; Dako, Glostrup, Denmark), p63 [DAK‐p63, ready to use (RTU), Dako], p40 (polyclonal rabbit antibody, RTU, Biocare Medical, Pacheco, CA, USA), AFF2 (polyclonal rabbit antibody, 1:25 dilution; Atlas Antibodies AB, Stockholm, Sweden), SOX10 (SP267, RTU; Cell Marque, Rocklin, CA, USA), S100 protein (polyclonal rabbit antibody, RTU; Dako).

Techniques: Biomarker Discovery, Extraction, Dissection

Journal: Histopathology

Article Title: Sinonasal adenosquamous carcinomas arising in seromucinous hamartoma or respiratory epithelial adenomatoid hamartoma with atypical features: Report of five detailed clinicopathological and molecular characterisation of rare entity

doi: 10.1111/his.15369

Figure Lengend Snippet: In some of the fragments, the atypical sinonasal glands arising in seromucinous hamartoma (ASGSH) changes were advanced, with evidence of transformation to an aggressively appearing adenosquamous carcinoma (ASC) ( A–C ) in which the glandular component predominated over the squamous keratinising component ( A ). Immunohistochemically, SOX10 was positive in the seromucinous hamartoma (SH) component only ( D ). The p63 and p40 stained only scattered residual myoepithelial cells in the SH component and were densely expressed in respiratory epithelial adenomatoid hamartoma (REAH), ASGSH and ASC parts ( E ). The protooncogene marker p16 was highly expressed in atypical glands and ASC ( F ). [Color figure can be viewed at wileyonlinelibrary.com ]

Article Snippet: The following antibodies were used: p16 (R15A, rabbit monoclonal antibody, 1:100 dilution; DB Biotech, Kosice, Slovakia), CK7 (OV‐TL 12/30, 1:200 dilution; Dako, Glostrup, Denmark), p63 [DAK‐p63, ready to use (RTU), Dako], p40 (polyclonal rabbit antibody, RTU, Biocare Medical, Pacheco, CA, USA), AFF2 (polyclonal rabbit antibody, 1:25 dilution; Atlas Antibodies AB, Stockholm, Sweden), SOX10 (SP267, RTU; Cell Marque, Rocklin, CA, USA), S100 protein (polyclonal rabbit antibody, RTU; Dako).

Techniques: Transformation Assay, Staining, Marker

Journal: Histopathology

Article Title: Sinonasal adenosquamous carcinomas arising in seromucinous hamartoma or respiratory epithelial adenomatoid hamartoma with atypical features: Report of five detailed clinicopathological and molecular characterisation of rare entity

doi: 10.1111/his.15369

Figure Lengend Snippet: The malignant component was focally keratinising adenosquamous carcinoma (ASC) ( A ), invading the cartilage ( B ) and striated muscle ( C ). The p16 proto‐oncogene was also positive in both the dysplastic epithelium and ASC ( D ). Cytokeratin‐7 (CK7) was positive in respiratory epithelial adenomatoid hamartoma (REAH), seromucinous hamartoma (SH) (middle), the luminal part of atypical sinonasal glands arising in SH (ASGSH) (right) and the adenocarcinoma component (left) ( E ). In contrast, p63 showed expression in the abluminal part of REAH, was reduced in scattered residual myoepithelial cells in seromucinous hamartoma (SH) (left), was positive in the abluminal atypical part of ASGSH (right) and was well expressed in ASC ( F ). [Color figure can be viewed at wileyonlinelibrary.com ]

Article Snippet: The following antibodies were used: p16 (R15A, rabbit monoclonal antibody, 1:100 dilution; DB Biotech, Kosice, Slovakia), CK7 (OV‐TL 12/30, 1:200 dilution; Dako, Glostrup, Denmark), p63 [DAK‐p63, ready to use (RTU), Dako], p40 (polyclonal rabbit antibody, RTU, Biocare Medical, Pacheco, CA, USA), AFF2 (polyclonal rabbit antibody, 1:25 dilution; Atlas Antibodies AB, Stockholm, Sweden), SOX10 (SP267, RTU; Cell Marque, Rocklin, CA, USA), S100 protein (polyclonal rabbit antibody, RTU; Dako).

Techniques: Expressing

Journal: Chemical reviews

Article Title: Oxygen Activation by Cu LPMOs in Recalcitrant Carbohydrate Polysaccharide Conversion to Monomer Sugars

doi: 10.1021/acs.chemrev.7b00421

Figure Lengend Snippet: Fungal Species of Industrial Relevance with a Focus on Cellulosic Biofuels

Article Snippet: 134 – 136 highlights a few species of particular industrial relevance, especially with regard to saccharification of lignocellulosic biomass. table ft1 table-wrap mode="anchored" t5 caption a7 species source LPMO genes details example commercial products Trichoderma reesei canvas bivouac tents WWII 137 3 established enzyme production host 138 Spezyme CP (DuPont) Celluclast (Novozymes) Aspergillus niger soil 8 used for commercial citric acid production E19 (Rohm and Haas) C6105, C1184 (Sigma-Aldrich) Rapidase Press (DSM) Myceliophthora thermophila compost piles 139 23–30 thermophilic, established enzyme production host 140 , 141 Fibrezyme G4 (DuPont) Thermoascus aurantiacus self-heating hay 142 3 thermophilic, proposed as enzyme production host 143 Rasamsonia emersonii (Talaromyces emersonii) self-heating wood chip pile 144 2 thermophilic Filtrase NL (DSM) Open in a separate window Fungal Species of Industrial Relevance with a Focus on Cellulosic Biofuels Many industrially relevant fungi that have been studied for their capability to degrade lignocellulosic biomass substrates encode LPMOs in their genomes.

Techniques: