ํฌ๊ธฐ ์ ํ
์ ํ์ ๋ณด (DICE ๋ฐฐ์ก ์ ๋น์ฉ ๋ณ๋)
์ ํ ์ด๋ฆ
Anti-Microtubule-Associated Protein 2 (MAP2) Antibody, Chemiconยฎ, from rabbit
biological source
rabbit
antibody form
saturated ammonium sulfate (SAS) precipitated
antibody product type
primary antibodies
clone
polyclonal
species reactivity
rat, mouse, human
manufacturer/tradename
Chemiconยฎ
technique(s)
ELISA: suitable, immunocytochemistry: suitable, immunohistochemistry (formalin-fixed, paraffin-embedded sections): suitable, western blot: suitable
NCBI accession no.
UniProt accession no.
target post-translational modification
unmodified
Quality Level
Gene Information
human ... MAP2(4133)
mouse ... Map2(17756)
rat ... Map2(25595)
์ ์ฌํ ์ ํ์ ์ฐพ์ผ์ญ๋๊น? ๋ฐฉ๋ฌธ ์ ํ ๋น๊ต ์๋ด
General description
Immunogen
Application
1:1,000 dilution of a previous lot was used on primary neurons.
Immunohistochemistry:
1:1,000 dilution on 4% paraformaldehyde / PBS fixed tissue sections.
Immunoblot:
1:2,000 dilution was used on a previous lot. Recognizes MAP2A (280-300kDa, and MAP2B (270-280KDa), and to a lesser extent MAP2C (70kDa) and MAP2D (70-75kDa).
ELISA:
greater than or equal to1:2,000 dilution of a previous lot was used.
Optimal working dilutions must be determined by the end user.
Neuroscience
Neuronal & Glial Markers
Neurofilament & Neuron Metabolism
Biochem/physiol Actions
Physical form
Preparation Note
Analysis Note
Human brain tissue or human glioblastoma T98G cells
MAP2 (cat. # AB5622) staining on Normal Cerebellum. Tissue pretreated with Citrate, pH 6.0. This lot of antibody was diluted to 1:500, using IHC-Select Detection with HRP-DAB. Immunoreactivity is seen as fiber-like- staining (brown) on microtubule.
Optimal Staining With TE Buffer, pH 9.0, Epitope Retrieval: Human Cerebellum
Legal Information
Disclaimer
์ ํฉํ ์ ํ์ ์ฐพ์ ์ ์์ผ์ ๊ฐ์? ย
๋น์ฌ์ ์ ํ ์ ํ๊ธฐ ๋๊ตฌ.์(๋ฅผ) ์๋ํด ๋ณด์ธ์.
์ ์ฅ ๋ฑ๊ธ
12 - Non Combustible Liquids
wgk
nwg
flash_point_f
Not applicable
flash_point_c
Not applicable
์ํ ์ฑ์ ์(COA)
์ ํ์ ๋กํธ/๋ฐฐ์น ๋ฒํธ๋ฅผ ์ ๋ ฅํ์ฌ ์ํ ์ฑ์ ์(COA)์ ๊ฒ์ํ์ญ์์ค. ๋กํธ ๋ฐ ๋ฐฐ์น ๋ฒํธ๋ ์ ํ ๋ผ๋ฒจ์ ์๋ โ๋กํธโ ๋๋ โ๋ฐฐ์นโ๋ผ๋ ์ฉ์ด ๋ค์์ ์ฐพ์ ์ ์์ต๋๋ค.
์ด ์ ํ์ ์ด๋ฏธ ๊ฐ์ง๊ณ ๊ณ์ญ๋๊น?
๋ฌธ์ ๋ผ์ด๋ธ๋ฌ๋ฆฌ์์ ์ต๊ทผ์ ๊ตฌ๋งคํ ์ ํ์ ๋ํ ๋ฌธ์๋ฅผ ์ฐพ์๋ณด์ธ์.
๊ด๋ จ ์ฝํ ์ธ
Thereโs so much room for experimental variability in traditional immunodetection workflows. For your peace of mind โ and ours โ we designed the SNAP i.d.ยฎ 2.0 system to streamline your Western blot and immunohistochemistry experiments. The concept is simple: a vacuum-driven flow of blocking, antibody, and washing solutions reduces slide and membrane handling. That means a lot less shaking, dipping, pouring and waiting. And now you can process multiple blots and slides in parallel, so itโs easy to apply consistent conditions across experiments.
๊ตญ์ ๋ฌด์ญ ํ๋ชฉ ๋ฒํธ
| SKU | GTIN |
|---|---|
| AB5622 | 04053252671319 |
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