제품 이름
Anti-acetyl-alpha tubulin Antibody, clone 6-11B-1, clone 6-11B-1, from mouse
biological source
mouse
antibody form
purified immunoglobulin
antibody product type
primary antibodies
clone
6-11B-1, monoclonal
species reactivity
sea urchin, bovine, monkey, Chlamydomonas, Drosophila, mouse, rat-kangaroo, human
technique(s)
dot blot: suitable
electron microscopy: suitable
immunocytochemistry: suitable
western blot: suitable
isotype
IgG2bκ
GenBank accession no.
UniProt accession no.
shipped in
wet ice
target post-translational modification
acetylation (Lys40)
Quality Level
Gene Information
human ... TUBA1A(7846)
Analysis Note
Western Blotting Analysis: 4.0 µg/mL of this antibody detected acetyl-alpha tubulin in 10 µg of HeLa cell lysate.
Application
Cell Structure
Adhesion (CAMs)
Immunocytochemistry Analysis: A representative lot detected acetylated alpha-tubulin in cultured normal human kidney epithelial cells (Courtesy of Dr Christopher Ward, University of Kansas Medical Center).
Western Blotting Analysis: A representative lot detected alpha-tubulin in sea urchin sperm axoneme lysates, but not in lysates from taxol-stabilized microtubules from sea urchin eggs (Piperno, G., and Fuller, M. (1985). J Cell Biol.101(6):2085-2094).
Dot Blot Analysis: A representative lot detected alpha-tubulin in both the ionic detergent Sarkosyl-soluble and insoluble fractions from sea urchin spern axoneme extracts (Piperno, G., and Fuller, M. (1985). J Cell Biol.101(6):2085-2094).
Immunocytochemistry Analysis: A representative lot detected acetylated and deacetylated, but not unacetylated alpha-tubulin in COS-7 green monkey kidney fibroblasts and Ptk2 rat kangaroo kidney epithelial cells by fluorescent immunocytochemistry (Soppina V., et al. (2012). PLoS One. 7(10):e48204).
Electron Microscopy Analysis: The Fab fragment of clone 6-11B-1 has been shown to stain Taxol-stabilized microtubules polymerized in vitro from purified bovine brain tubulin with or without SIRT2-catalyzed deacetylation (Soppina V., et al. (2012). PLoS One. 7(10):e48204).
Biochem/physiol Actions
Disclaimer
General description
Immunogen
Other Notes
Physical form
Preparation Note
Legal Information
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저장 등급
12 - Non Combustible Liquids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
관련 콘텐츠
A major focus of breast cancer research is to understand the mechanisms responsible for disease progression and drug resistance. Toward that end, it has been found that approximately two thirds of all human breast carcinomas overexpress the Estrogen Receptor α (ERα) protein and it remains the primary pharmacological target for endocrine therapy1,2. The normal cellular function of ERα is as a transcription factor that mediates a wide variety of physiological processes, many of which are dependent upon phosphorylation of the receptor at specific amino acid residues3,4. Indeed, ERα is known to be phosphorylated at a multitude of different sites, yet how these all correlate to disease remains unclear5. Here, we interrogated multiple sites of ERα for phosphorylation status by screening an extensive panel of different breast cancer patient samples and other non-breast cancer tissue microarray (TMA) slide samples to determine their relevance to disease.
국제 무역 품목 번호
| SKU | GTIN |
|---|---|
| MABT868 | 04055977277050 |
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