Application
凝胶过滤标记物用于蛋白质层析和凝胶过滤层析。凝胶过滤标记已被用于研究糖皮质激素诱导的淋巴细胞溶解，作为免疫系统内细胞凋亡的模型系统。凝胶过滤标记也用于分离 玉竹 凝集素，其对 Vero 细胞显示出显著的抗 HSV-II 活性，对人黑色素瘤 A375 细胞具有细胞毒性，并以半胱天冬酶依赖性方式诱导细胞凋亡。
General description
凝胶过滤标记试剂盒包含5瓶蛋白和1瓶蓝色葡聚糖，以用于校准。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Cristina L Marolda et al.
Journal of bacteriology, 190(6), 2128-2137 (2008-01-22)
Wzz is a membrane protein that determines the chain length distribution of the O-antigen lipopolysaccharide by an unknown mechanism. Wzz proteins consist of two transmembrane helices separated by a large periplasmic loop. The periplasmic loop of Escherichia coli K-12 Wzz
Andreas Krug et al.
The Journal of biological chemistry, 280(1), 585-595 (2004-10-21)
In Corynebacterium glutamicum, the activity of aconitase is 2.5-4-fold higher on propionate, citrate, or acetate than on glucose. Here we show that this variation is caused by transcriptional regulation. In search for putative regulators, a gene (acnR) encoding a TetR-type
Ulrich Strych et al.
BMC microbiology, 7, 40-40 (2007-05-19)
Over the past fifteen years, antibiotic resistance in the Gram-positive opportunistic human pathogen Streptococcus pneumoniae has significantly increased. Clinical isolates from patients with community-acquired pneumonia or otitis media often display resistance to two or more antibiotics. Given the need for
Daisuke Seo et al.
Biochimica et biophysica acta. Bioenergetics, 1861(3), 148140-148140 (2019-12-16)
Among the thioredoxin reductase-type ferredoxin-NAD(P)+ oxidoreductase (FNR) family, FNR from photosynthetic purple non‑sulfur bacterium Rhodopseudomonas palustris (RpFNR) is distinctive because the predicted residue on the re-face of the isoalloxazine ring portion of the FAD prosthetic group is a tyrosine. Here
Michael Bussmann et al.
The Journal of biological chemistry, 285(38), 29305-29318 (2010-07-21)
The cg1324 gene (rosR) of Corynebacterium glutamicum encodes a MarR-type transcriptional regulator. By a comparative transcriptome analysis with DNA microarrays of a ΔrosR mutant and the wild type and subsequent EMSAs with purified RosR protein, direct target genes of RosR
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