
荧光标记,乙酰化赖氨酸抗体(Acetyl Lysine An
tibody,FITC)- 询价
- immunechem
- IP0385
- 加拿大
- 2025年07月05日
- 兔源
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- 标记物:
FITC
- 是否单克隆:
2
- 宿主:
兔源
- 库存:
大量
- 抗原来源:
合成多肽
- 规格:
100ug
Description: Affinity purified rabbit polyclonal anti-acetylated lysine antibodies. It was developed using a unique technique that utilizes the acetylated KLH as immunogen and the acetylated lysine-specific antibodies. It was specifically purified with immobilized acetylated lysine on agarose. The purified antibody is conjugated to fluorescein isothiocyanate
Species: Rabbit
Formulation: 250 µg/mL antibody stored in PBS, pH 7, with 50% glycerol
Storage & Stability: Store product at –20℃. Three years from date of shipping.
Immunogen: Acetylated KLH conjugates
Conjugation: FITC/Ab ratio 10:1, followed by G25 filtration.
Purification: The antibody was purified on acetyl-lysine agarose.
Specificity: Recognize proteins acetylated on lysine residues.
Tested: acetylated histone, acetylated BSA, and acetylated MBP, no reaction to the non-acetylated proteins.
Application: For direct immunofluorescence experiments
Scientific Background: Acetylation of lysine is an important reversible modification. The activities of some proteins are controlled by acetylation of lysine. Histone acetyltransferases (HATs) acetylate the conserved amino-terminal domains of the four core histones (H2A, H2B, H3 and H4) that contain lysines residues. Histone deacetylases (HDACs) removes the acetyl group from the same residue. [1] Acetylation/deacetylation of histones results in cell signaling processes that include gene activity, cell growth, differentiation and apoptosis. [2] In cancer and polyglutamine diseases, the regulation of protein acetylation/deacetylation is impaired (7). Numerous anti-cancer drugs target HDACs. [3]
References: 1. Hassig, C.A. et al. Curr. Opin. Chem. Biol. 1997. 1, 3, 300-308. 2. Allfrey, V. G. et al. Proc. Natl. Acad. Sci. USA 1964, 51, 786-794. 3. Vigushin, D.M. et al. Curr. Cancer Drug Targets 2004, 4, 205-218.
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文献和实验Protocols for Lysine Conjugation
Currently, the most widely used chemical methodology for the conjugation of drugs to monoclonal antibodies involves either lysine or cysteine residues. In this chapter, several methods for the preparation of antibody–drug conjugates (ADCs
Angew. Chem:刘涛 / 罗小舟 / 刘小云团队在组蛋白表观遗传学研究中取得进展
基酸(Non-canonical Amino Acid,ncAA)编码到宿主目标蛋白的特定位点上。 首先,研究人员汇总了现有的酿酒酵母基因密码子扩展体系(包括 PylRS 和 E.coli LeuRS 体系),将 EGFP 的荧光信号强度作为 GCE 体系编码效率的评估指标,并构建了一系列 GCE 体系,比较这些体系将乙酰赖氨酸(Acetyl-lysine,AcK)插入到 EGFP 特定位点的效率,从中筛选出插入效率高且正交的 GCE 体系——PLRS/4xtRNALeu 对(图 2a)。同时研究
How Do I make an Antibody against a Peptides
-Activated Carrier Proteins (Figure 1). If your hapten does not have a sulfhydryl group, you can use EDC chemistry (Figure 2) to couple amines (lysine) or carboxylic acids (glutamic, aspartic acid or 5'-phosphate) to the carrier protein. Keyhole limpet
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