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marble counter top. Very flat verified by the granite tables at my old job. I measure all frames and forks from both sides to have redundant measurement. I never trust just one side of the bb shell. The standoff is machined flat on both sides and can clamp to any part of the table. No holes.
SET 1 – HLT Remodel: 4-20-2023
We’ll keep exploring the new electronics area here in a moment, but I wanted to briefly spin around first and show y’all the new center actionway of the store, which at this point had become fully completed! Remember, this entire actionway was shifted, and as you might can guess, the ultimate goal of that work was so that it would make the new electronics department visible even from the front end of the store (as it aligns perfectly with this actionway). You can see some swaths of empty space towards the middle of the pic where the blue world departments hadn’t yet shifted to accommodate their new extra space; and on my left, we actually (finally!) get to see a tiny portion of the temporarily relocated storage bin/trash can shelving, placed atop the former shoe department carpeting (surprisingly one of only two good views I ever got of this…)
(c) 2024 Retail Retell
These places are public so these photos are too, but just as I tell where they came from, I'd appreciate if you'd say who :)
This little U-shaped slot holds the magazine drum in place and centered in the receiver. Magnets hold it in place, but this keeps it from being knocked around.
The Moon rises and the Sun sets on opposing sides of the Burton Memorial Tower at the University of Michigan, Ann Arbor, in early March, 2023.
Consensus phylogenetic tree of the NCLDVs.
Bayesian phylogenetic tree was constructed from a cured concatenated alignment of 4 universal NCVOGs (496 conserved positions), including CroV corresponding proteins: primase-helicase (NCVOG0023), DNA polymerase (NCVOG0038), packaging ATPase (NCVOG0249), and A2L-like transcription factor (NCVOG0262). Bayesian posterior probabilities are mentioned near branches as a percentage and are used as confidence values of tree branches. Only probabilities at major nodes are shown. Scale bar represents the number of estimated changes per position for a unit of branch length. Abbreviated names for NCLDVs: b1_Helvi, Heliothis virescens ascovirus 3e; b1_Spofr, Spodoptera frugiperda ascovirus 1a; b1_Trini, Trichoplusia ni ascovirus 2c; c1_Afrsw, African swine fever virus; l1_Aedta, Aedes taeniorhynchus iridescent virus (Invertebrate iridescent virus 3); l2_Invir, Invertebrate iridescent virus 6; l3_Lymch, Lymphocystis disease virus - isolate China; l3_Lymdi, Lymphocystis disease virus 1; l4_Infsp, Infectious spleen and kidney necrosis virus; l5_Ambti, Ambystoma tigrinum virus; l5_Frovi, Frog virus 3; l5_Singr, Singapore grouper iridovirus; m6_Masvi, Marseille virus; q1_Acatu, Acanthocystis turfacea Chlorella virus 1; q1_ParAR, Paramecium bursaria Chlorella virus AR158; q1_Parbu, Paramecium bursaria Chlorella virus 1; q1_ParFR, Paramecium bursaria Chlorella virus FR483; q1_ParMT, Paramecium bursaria chlorella virus MT325; q1_ParNY, Paramecium bursaria Chlorella virus NY2A; q2_Emihu, Emiliania huxleyi virus 86; q3_Ectsi, Ectocarpus siliculosus virus 1; q3_Felsp, Feldmannia species virus; q6_Ostvi, Ostreococcus virus OsV5; u1_Bovpa, Bovine papular stomatitis virus; u1_Canvi, Canarypox virus; u1_Crovi, Crocodilepox virus; u1_Deevi, Deerpox virus W-848-83; u1_Fowvi, Fowlpox virus; u1_Goavi, Goatpox virus Pellor; u1_Lumsk, Lumpy skin disease virus NI-2490; u1_Molco, Molluscum contagiosum virus; u1_Myxvi, Myxoma virus; u1_Orfvi, Orf virus, complete genome; u1_Rabfi, Rabbit fibroma virus; u1_Shevi, Sheeppox virus 17077-99; u1_Swivi, Swinepox virus; u1_Tanvi, Tanapox virus; u1_Vacvi, Vaccinia virus; u1_Varvi, Variola virus (smallpox virus); u1_Yabli, Yaba-like disease virus; u1_Yabmo, Yaba monkey tumor virus; u2_Amsmo, Amsacta moorei entomopoxvirus; u2_Melsa, Melanoplus sanguinipes entomopoxvirus.
Merrivale
Northern length of the alignment. View from the east (Scale 1m).
stonerows.wordpress.com/gazetteer/region/dartmoor/merriva...
Moon, Jupiter and Venus Having Fun in the sky, as seen in Israel.
No idea which one is which, But it's still beautiful to look at (-:
01/12/08, 6:30 PM
Amino acid sequence alignment and phylogenetic analysis of CsVDE and homologous proteins.(A) Schematic description of CsVDE domains. (B) Alignment of the deduced amino acid sequences of VDE in different plants. Red lines indicate the VDE Cys-rich domain; Gray lines indicate the Lipocalins domain; Blue lines indicate the Glu-rich domain. The important residues for pH switch are marked with black stars and the putative active site residues with black squares reference from Arnoux et al. (2009) [11]. Arabidopsis thaliana VDE (accession No. AEE28305), Zingiber officinale VDE (accession No. AAX59986), Lactuca sativa VDE (accession No. AAC49373), Nicotiana tabacum VDE (accession No. AAC50031), Coffea arabica VDE (accession No. ABB70816) sequences are shown. Black indicates 100% homology of the amino acid. Red indicates 75% homology of the amino acid. Green indicates 50% homology of the amino acid. (C) Phylogenetic analyses of selected VDEs. Phylogenetic studies were carried out using MrBayes3.1.2 and viewed with the TreeView package. All the trees were obtained with 200,000 generations for the chains, a sample frequency of a 10, and a burn in of 5,000 (ngen = 200000; Samplefreq = 10; burnin = 5,000). Camellia sinensis VDE (accession No. AAL67858), Vitis vinifera VDE (accession No. XP_002267152), Osterococcus tauri VDE (accession No. XP_003083515), Ostreococcus lucimarinus VDE (accession No. XP_001421704), Micromonas sp. VDE (accession No. XP_002503106), Micromonas pusilla VDE (accession No. XP_003061123), Ectocarpus siliculosus VDE (accession No. CBJ26509), Phaeodactylum tricornutum VDE (accession No. XP_002178643), Oryza sativa Japonica Group VDE (accession No. AAL83562), Zea mays VDE(accession No. NP_001147756), Solanum lycopersicum VDE (accession No. ACM92036).
You may see layer alignment issues on prints with flat surfaces; notice how the print on the left exhibits the problem very well but the contour of the print on the right masks the problem to a certain degree. This can be caused by a variety of issues, but here are some of the things you can do to get more consistency:
1. Slow down if using non-Marlin firmware. Print your perimeter at 20-25 mm/sec
2. Tighten your belts.
3. Make sure any springs on your build platform are very tight and that the top plate can't wobble around independent of the bottom plate.
4. Upgrade your Z-coupling to a better one, such as www.thingiverse.com/thing:11220
5. Replace any non-straight threaded rod used in the Z-axis with perfectly straight ones.
6. Unless they were printed perfectly, replace your timing pulleys with manufactured ones, such as sdp-si.com/eStore/PartDetail.asp?Opener=Group&PartID=...
Sequence analysis of eukaryotic and prokaryotic SLC1 transporters.(A) Sequence alignment of TMD8 region from human, insect, bacterial, and archael transporters. CuqDCT, CuqEAAT, AeaDCT, and AeaEAAT represent the EAAT and DCT orthologs from Culex quinquefasciatus and Aedes aegypti, respectively. AngEAAT1 and AngEAAT2 represent the transporters from Anopheles gambiae. Drosophila EAAT1/2 are from Drosophila melanogaster, Gltph from Pyrococcus horikoshii, and DctA is from Bacillus subtilis. Highlighted TMD8 residues involved in substrate binding are labeled above using human EAAT3 numbering. R447 and N451 are conserved in all EAAT-like orthologs, while D444 and T448 are changed to asparagine and alanine, respectively in the CuqDCT and AeaDCT mosquito transporters. Sequence alignments were performed with ClustalX2 and Jalview. (B) The phylogenetic relationship of the EAAT and DCT proteins from Culex quinquefasciatus and Aedes aegypti mosquito species together with the two EAATs from Drosophila (ClustalX2 based alignment).