ํฌ๊ธฐ ์ ํ
์ ํ์ ๋ณด (DICE ๋ฐฐ์ก ์ ๋น์ฉ ๋ณ๋)
์ ํ ์ด๋ฆ
Anti-Tyrosine Hydroxylase Antibody, Chemiconยฎ, from rabbit
biological source
rabbit
antibody form
affinity isolated antibody
antibody product type
primary antibodies
clone
polyclonal
purified by
affinity chromatography
species reactivity
human, mollusk, feline, ferret, Aplysia (marine mollusc), rat, squid, Drosophila, mouse
manufacturer/tradename
Chemiconยฎ
technique(s)
ELISA: suitable, immunofluorescence: suitable, immunohistochemistry (formalin-fixed, paraffin-embedded sections): suitable, immunoprecipitation (IP): suitable, western blot: suitable
NCBI accession no.
UniProt accession no.
shipped in
dry ice
target post-translational modification
unmodified
Quality Level
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General description
Immunogen
Application
A previous lot of this antibody was uesd at 1:100-1:1,000 dilution, 4ยฐC, for 1-3 days. Stains both fresh frozen and paraffin embedded tissue samples by indirect immunofluorescence and immunoperoxidase.
Immunofluorescence:
A previous lot of this antibody was used at 1:100-1:1,000 dilution.
Immunoprecipitation:
A previous lot of this antibody was used on Immunoprecipitation.
ELISA:
A previous lot of this antibody was used in ELISA.
Optimal dilutions must be determined by the end user.
Neuroscience
Neurotransmitters & Receptors
Neuronal & Glial Markers
Biochem/physiol Actions
Physical form
Preparation Note
Analysis Note
POSITIVE CONTROL: Brain (corpus striatum, sympathetic nerve terminals) and adrenal glands.
NEGATATIVE CONTROL: Liver.
Western Blot Analysis:
1:1000 dilution of this lot detected tyrosine hydroxylase on 10 ฮผg of PC12 lysates.
Legal Information
Disclaimer
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์ ์ฅ ๋ฑ๊ธ
10 - Combustible liquids
์ํ ์ฑ์ ์(COA)
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๋ฌธ์
Antibodies combine with specific antigens to generate an exclusive antibody-antigen complex. Learn about the nature of this bond and its use as a molecular tag for research.
Learn differences in monoclonal vs polyclonal antibodies including how antibodies are generated, clone numbers, and antibody formats.
Immunofluorescence uses antibody-conjugated fluorescent molecules for protein localization, modification confirmation, and protein complex visualization.
Explore the basics of working with antibodies including technical information on structure, classes, and normal immunoglobulin ranges.
ํ๋กํ ์ฝ
Tips and troubleshooting for FFPE and frozen tissue immunohistochemistry (IHC) protocols using both brightfield analysis of chromogenic detection and fluorescent microscopy.
๊ด๋ จ ์ฝํ ์ธ
Find protein research tools to prepare, isolate, and analyze proteins. Organized by how to extract, protect, purify, enrich, modify, and quantify proteins.
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 |
|---|---|
| AB152 | 04053252287138 |
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