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Commit eb55afa0 authored by Lucy Hao's avatar Lucy Hao :moyai:
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get new svg half logo

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......@@ -127,13 +127,6 @@ body {
}
}
.title {
font-size: 100px;
@media only screen and (max-width: 768px) {
font-size: 40px;
}
}
.header-logo {
height: 33vh;
@media only screen and (max-width: 768px) {
......
import * as React from "react";
import { headerFont } from "@/utils/fonts";
import styled from "styled-components";
const Title = styled.h1`
font-size: 90px;
@media only screen and (max-width: 768px) {
font-size: 40px;
}
`;
const Header = ({ title, subtitle, white }) => (
<div
className="flex-row"
style={{
paddingTop: "15vh",
paddingBottom: "15vh",
overflowWrap: "break-word",
width: "fit-content",
paddingLeft: "10%",
paddingRight: "10%",
height: "60vh",
width: "80vw",
margin: "auto",
}}
id="header"
>
<div className="half-mask">
<div className="center-text flex-row">
<img
src="https://static.igem.wiki/teams/4796/wiki/figma-assets/logo-svg.svg"
src="https://static.igem.wiki/teams/4796/wiki/half-svg.svg"
alt="Logo"
className="header-logo"
style={{ margin: "auto", justifyItems: "space-between" }}
/>
</div>
<div className="center-text">
<h1
className={
"title" + " " + headerFont.className + (!white && " gradient-header")
}
<Title
className={headerFont.className + (!white && " gradient-header")}
style={{
letterSpacing: ".2rem",
margin: 0,
margin: "auto",
wordBreak: "break-word",
textTransform: "uppercase",
}}
>
<strong>{title}</strong>
</h1>
</Title>
<p className="subtitle"> {subtitle}</p>
</div>
</div>
......
......@@ -78,9 +78,7 @@ extracellular dna nuclease could have degraded plasmid DNA. We decided
to switch to electroporation protocols as we were repeatedly
unsuccessful with chemical transformations.
#### Protocol Iteration #3 Electroporation using sucrose method adapted
from Weinstock et al[^2]
#### Protocol Iteration #3 Electroporation using sucrose method adapted from Weinstock et al[^2]
1. Grow *V. natriegens* culture at 37 °C in a baffled flask with shaking at 200 r.p.m. until an OD600 of 0.5.
2. Split the culture into two chilled 250-mL centrifuge bottles and incubate on ice for 15 min
......
......@@ -95,7 +95,6 @@ Our team led a workshop focused on **teaching core microbiology concepts** throu
<Figure
src="https://static.igem.wiki/teams/4796/wiki/inclusivity/image1.jpg"
long
num="1"
caption="Our team and C.O.D.E member explaining agar art."
/>
......@@ -104,7 +103,6 @@ The workshop was adapted to ensure that there was room for lots of question aski
<Figure
src="https://static.igem.wiki/teams/4796/wiki/inclusivity/image2.jpg"
long
num="2"
caption="Our team members at the iGEM x C.O.D.E day."
/>
......@@ -115,7 +113,6 @@ In addition to immersing neurodivergent individuals into the world of synbio, th
<Figure
src="https://static.igem.wiki/teams/4796/wiki/inclusivity/image3.jpg"
long
num="3"
caption="Our team members at the iGEM x C.O.D.E day."
/>
......@@ -132,9 +129,9 @@ ithin the diversity of Vancouver, there is an important focus on the revelation
<Figure
src="https://static.igem.wiki/teams/4796/wiki/inclusivity/image4.png"
long
num="4"
caption="An example of the University of British Columbia acknowledging Indigenous land. Derived from Musqueam & UBC - Indigenous Portal"
alternate
/>
To honour the First Nations populations, we have decided that an important direction for initiatives within future iGEM seasons is to highlight the recognition of barriers and stolen work presented in a webinar to inform our academic space of the the Equity, Diversity, and Inclusivity (EDI) that is required in order to open opportunities for Indigenous work in the science space from a cultural perspective.
......
......@@ -4,6 +4,7 @@ import Head from "next/head";
import Link from "next/link";
import Newspapers from "@/components/landingpage/Newspapers";
import PillarsLanding from "@/components/landingpage/PillarsLanding";
import RotatingImages from "@/components/RotatingImages";
export default function Page() {
return (
......@@ -16,6 +17,7 @@ export default function Page() {
</div>
{/* landing page starts */}
<RotatingImages />
<Newspapers />
<PillarsLanding />
......
......@@ -334,13 +334,6 @@ system are greater than each of the plasmids individually, confirming
the restoration of mCherry-XL fluorescence and thus the success of our
split intein mechanism in CFPS.
<Figure
alternate
num="15"
caption="CFPS reaction fluorescence growth curve measured at 558/589 nm, normalized against no plasmid control."
src="https://static.igem.wiki/teams/4796/wiki/results/image4.png"
/>
[^1]:
Weinstock MT, Hesek ED, Wilson CM, Gibson DG. Vibrio natriegens as
a fast-growing host for molecular biology. Nature Methods. 2016 Oct
......
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