推荐产品
产品名称
聚-D-赖氨酸 氢溴酸盐, mol wt ≥300,000
表单
powder or solid
质量水平
分子量
≥300,000
技术
cell culture | mammalian: suitable
颜色
white to off-white
储存温度
−20°C
SMILES字符串
O=C(C)[C@@](NC)([H])CCCCN.[Br]
InChI
1S/C6H14N2O2.BrH/c7-4-2-1-3-5(8)6(9)10;/h5H,1-4,7-8H2,(H,9,10);1H
InChI key
MEXAGTSTSPYCEP-UHFFFAOYSA-N
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应用
聚-D-赖氨酸聚合物可用于制备细胞附着的表面。D-赖氨酸聚合物也可用于消化聚-L-赖氨酸聚合物并导致L-赖氨酸过量摄取的细胞。
建议使用0.5 - 1.0 mL的该产品0.1 mg/mL溶液用作细胞培养的基质对25 cm2进行涂覆。 较低分子量的该产品粘度相对较低,但较高分子量的形式则可提供每分子更多的附着位点。
建议使用0.5 - 1.0 mL的该产品0.1 mg/mL溶液用作细胞培养的基质对25 cm2进行涂覆。 较低分子量的该产品粘度相对较低,但较高分子量的形式则可提供每分子更多的附着位点。
生化/生理作用
多聚-L-赖氨酸(PDL)氢溴酸盐是细胞的非特异性粘附因子,它通过增强细胞膜表面的负电荷离子与培养表面之间的静电相互作用,促进细胞与固相基质的粘附。 当被细胞培养表面吸收后,聚-D-赖氨酸可增加带正电的细胞结合位点数量。
组分
聚-D-赖氨酸是一种带正电的氨基酸聚合物,其中每个赖氨酸残基约有一个HBr。 氢溴酸盐可使聚-D-赖氨酸呈可溶于水的结晶形式。 在β结构中可能会发现少量的产物,因为HBr干扰氨基与羧基或含N或O部分之间的氢键。
注意
无菌溶液可在2-8℃条件下稳定保存2年。脱水保存在-20°C条件下。
制备说明
本品分子量 > 30 万。为除去 HBr,将本品溶于中性缓冲液中,透析除去盐类。一般以本品为附着因子,在 5 mg 聚赖氨酸中加入 50 mL 无菌组织培养级水,每 25 cm2 溶液无菌涂布表面 1 mL。5 min 后,通过抽吸清除溶液,并彻底冲洗表面。在引入细胞和培养基前干燥两小时。
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
历史批次信息供参考:
分析证书(COA)
The EMBO journal, 39(22), e106249-e106249 (2020-09-22)
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Scientific reports, 10(1), 11047-11047 (2020-07-08)
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eLife, 9 (2020-11-11)
Microdeletions and microduplications of the 16p11.2 chromosomal locus are associated with syndromic neurodevelopmental disorders and reciprocal physiological conditions such as macro/microcephaly and high/low body mass index. To facilitate cellular and molecular investigations into these phenotypes, 65 clones of human induced
Biology of reproduction, 100(6), 1440-1452 (2019-03-15)
Nonhuman primates (NHPs) are considered to be the most valuable models for human transgenic (Tg) research into disease because human pathology is more closely recapitulated in NHPs than rodents. Previous studies have reported the generation of Tg NHPs that ubiquitously
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 25(10), 3426-3435 (2011-06-24)
Misfolding of the prion protein (PrP) is the central feature of prion diseases. The conversion of the normal α-helical PrP(C) into a pathological β-enriched PrP(Sc) constitutes an early event in the infectious process. Several hypotheses, involving different regions of the
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