SENI
KECANTIKAN & KESEHATAN
KERAJINAN
BUDAYA & SEJARAH
HIBURAN
LINGKUNGAN
MAKANAN & MINUMAN
REKAYASA BALIK
ILMU PENGETAHUAN
OLAHRAGA
TEKNOLOGI
PERANGKAT PAKAI

Staining: Making the Invisible Visible
The mounting rung ended on an awkward fact: a good mountant matches the refractive index of the tissue, and in doing so makes an unstained specimen almost invisible. You have removed the glare and the detail with it.
The fix arrived from an unexpected direction. The coal-tar dye industry of the 1860s and 70s — the same chemistry as the synthetic alizarin and Para red blueprints — produced hundreds of brilliant aniline dyes for textiles, and biologists discovered that they stained some cell structures and not others. Paul Ehrlich built a career on which dye went where, and in 1884 Hans Christian Gram found a sequence that split all bacteria into two groups by the structure of their cell walls.
A stain is not paint. It binds where the chemistry lets it bind, so WHERE it lands is itself the information.
Menengah
4 hours
Instruksi
1
1
Start with one dye and understand why it binds
Start with one dye and understand why it binds
Make a dilute methylene blue solution and put a drop on a scraping of onion or a smear of yeast. Within a minute the nuclei are blue and the rest is pale.
Methylene blue is a cation — a positively charged dye — and it is drawn to anything negatively charged. Nucleic acids are strongly negative, so the nucleus takes it up first and hardest. That is the whole logic of staining: match the charge or the chemistry of the dye to the structure you want, and the specimen sorts itself out.
Material untuk langkah ini:
Metilena biru10 ml
Bawang bombai1 buah
Ragi roti10 g
Kaca objek dengan kaca penutup20 buahAlat yang dibutuhkan:
Pipet berskala (Mohr)
Mikroskop2
2
Fix the smear before you stain it
Fix the smear before you stain it
Spread a thin smear, let it air-dry completely, then pass the slide briefly through a flame two or three times — warm, never hot.
Heat fixing does two things: it kills and sticks the material to the glass so it does not wash off during the staining steps, and it makes the cell membranes permeable so dye can get in. Overheat it and cells distort beyond recognition. The test is the back of your hand: the slide should feel warm, not painful.
Alat yang dibutuhkan:
Kaca objek dengan kaca penutup3
3
Run a Gram stain, in order, with the clock
Run a Gram stain, in order, with the clock
Crystal violet for one minute; rinse. Iodine for one minute; rinse. Then the decolouriser — alcohol — for a few SECONDS only; rinse at once. Finally safranin for a minute; rinse and blot dry.
The iodine is not a stain, it is a mordant: it forms a large complex with the crystal violet that is trapped inside a thick cell wall. The decolourising step is the entire test and it is the one that goes wrong — a few seconds too long and everything washes out and reads as Gram-negative. Time it. Do not guess.
Material untuk langkah ini:
Pewarna kristal violet50 ml
Kristal iodin5 g
Pewarna safranin50 ml
Etanol mutu laboratorium, 95 %100 mlAlat yang dibutuhkan:
Stopwatch
Sarung Tangan Nitril
Gelas Piala Borosilikat4
4
Read the result, and know what it means
Read the result, and know what it means
Purple cells are Gram-positive; pink or red cells are Gram-negative.
The difference is real structure, not a dye preference. A Gram-positive wall is a thick peptidoglycan mesh that holds the violet-iodine complex when the alcohol dehydrates and closes it. A Gram-negative wall is thin with an outer lipid membrane the alcohol dissolves, so the complex washes straight out and the safranin that follows is all you see. One minute of dye tells you something structural about an organism a thousand times too small to dissect.
Alat yang dibutuhkan:
Mikroskop5
5
Always run a known control alongside
Always run a known control alongside
Stain a slide of something you KNOW is Gram-positive on the same slide or alongside, in the same staining run.
Without it an all-pink result is ambiguous: either the organisms are Gram-negative, or you over-decolourised everything. The control answers that immediately, and it costs one extra smear. This is the same discipline as the dark control in the SODIS blueprint and the co-spot in the chromatography one — a result without a reference is a colour, not a finding.
Material untuk langkah ini:
Kaca objek dengan kaca penutup10 buahAlat yang dibutuhkan:
Mikroskop6
6
Counterstain, and use the whole palette
Counterstain, and use the whole palette
Try a two-dye scheme on plant sections: a dye that takes to lignified walls and a contrasting one for the cellulose, applied in sequence.
This is what haematoxylin and eosin do for animal tissue — one basic dye for the acidic nuclei, one acidic dye for the basic cytoplasm — and it is why almost every histology image you have ever seen is blue and pink. Two dyes that bind by opposite chemistry divide the specimen between them and nothing is left uncoloured.
Material untuk langkah ini:
Pewarna safranin50 ml
Metilena biru20 mlAlat yang dibutuhkan:
Gelas Piala Borosilikat
Stopwatch7
7
Dye uptake, time and the decolourising window
Dye uptake, time and the decolourising window
Memuat notebook Jupyter…
Alat yang dibutuhkan:
Stopwatch8
8
Treat the dyes with respect
Treat the dyes with respect
Wear gloves, work over a tray, and keep the dyes off skin and clothing. Label every bottle with what it is and when you made it.
Aniline dyes stain hands for days and fabric permanently, and several of the historic ones are now known to be harmful in ways their Victorian users had no idea about — which is worth remembering as a general lesson about materials, not only these. Made-up stains also go off: crystal violet precipitates and methylene blue oxidises, and an old stain that no longer works looks exactly like a technique failure.
Alat yang dibutuhkan:
Sarung Tangan NitrilBahan
8- 20 mlPlaceholder
- 1 buahPlaceholder
- 10 gPlaceholder
- Placeholder
- Placeholder
- Placeholder
- 100 mlPlaceholder
- Placeholder
Blueprint terkait
Blueprint ini berbagi pengetahuan — teknik, bahan, atau prinsip
CC0 Domain Publik
Cetak biru ini dirilis di bawah CC0. Anda bebas untuk menyalin, memodifikasi, mendistribusikan, dan menggunakan karya ini untuk tujuan apa pun, termasuk komersial, tanpa meminta izin.
Dukung Maker dengan membeli produk melalui Cetak Biru mereka di mana mereka mendapatkan Komisi Pembuat yang ditetapkan oleh Penjual, atau buat iterasi baru dari Cetak Biru ini dan masukkan sebagai koneksi di milik Anda sendiri.


