Thermo Fisher 710802 抗体,H3K79me2 Recombinant Polyclonal Antibody (8HCLC)/H3K79me2重组多克隆抗体(8HCLC)

2024-10-23

H3K79me2 Recombinant Polyclonal Antibody (8HCLC)/H3K79me2重组多克隆抗体(8HCLC)

货号:710802

规格:100 µg

价格:4809

产品类型:抗体和染料

品牌:Thermo Fisher

抗原:Peptide corresponding to Human HIST1H3A (aa 76-84)

物种:人

宿主:兔

抗体亚型:IgG

克隆号:8HCLC

荧光染料:其它

类型:多抗同型对照:
浓度: 0.5 mg/mL用法:2-3 µg/1x10^6 cells(ChIP);0.15-2.5 µg/mL(ELISA);1-2 µg/mL(WB)
产品详细信息This antibody is predicted to react with Pig, Rat, Monkey and Cat.Recombinant rabbit polyclonal antibodies are unique offerings from Thermo Fisher Scientific. They are comprised of a selection of multiple different recombinant monoclonal antibodies, providing the best of both worlds - the sensitivity of polyclonal antibodies with the specificity of monoclonal antibodies - all delivered with the consistency only found in a recombinant antibody. While functionally the same as a polyclonalantibody - recognizing multiple epitope sites on the target and producing higher detection sensitivity for low abundance targets - a recombinant rabbit polyclonal antibody has a known mixture of light and heavy chains. The exact population can be produced in every lot, circumventing the biological variability typically associated with polyclonal antibody production.靶标信息Histone H3 is one of the DNA-binding proteins found in the chromatin of all eukaryotic cells. H3 along with four core histone proteins binds to DNA forming the structure of the nucleosome. Histones play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. Post translationally, histones are modified in a variety of ways to either directly change the chromatin structure or allow for the binding of specific transcription factors. The N-terminal tail ofhistone H3 protrudes from the globular nucleosome core and can undergo several different types of post-translational modification that influence cellular processes. These modifications include the covalent attachment of methyl or acetyl groups to lysine and arginine amino acids and the phosphorylation of serine or threonine.
数据:

H3K79me2 Antibody (710802) in WBWestern blot analysis was performed on acid extracts (30 µg lysate) of HEK-293 (Lane 1), A549 (Lane 2), K562 (Lane 3) and HT-29 (Lane 4). The blots were probed with Anti-Histone H3K79me2 Recombinant Rabbit Polyclonal Antibody (Product # 710802, 1-2 µg/mL) and detected by chemiluminescence using Goat anti-Rabbit IgG (H+L) Superclonal™ Secondary Antibody, HRP conjugate (Product # A27036, 0.4 µg/mL, 1:2500 dilution). A 17 kDa band corresponding to Histone H3K79me2 was observed. To confirm the specificity of Anti- Histone H3K79me2 Recombinant Rabbit Polyclonal Antibody, competition was performed with the peptide (10 µg/mL) as shown in the corresponding blot on the right. The peptide competes with the antibody and prevents it from binding to the target protein. Known quantity of protein samples were electrophoresed using Novex® NuPAGE® 12% Bis-Tris gel (Product # NP0342BOX), XCell SureLock™ Electrophoresis System (Product # EI0002) and Novex® Sharp Pre-Stained Protein Standard (Product # LC5800). Resolved proteins were then transferred onto a nitrocellulose membrane with iBlot® Dry Blotting System (Product # IB21001). The membrane was probed with the relevant primary and secondary Antibody following blocking with 5% skimmed milk. Chemiluminescent detection was performed using Pierce™ ECL Western blotting Substrate (Product # 32106).

H3K79me2 Antibody (710802) in ChIPEnrichment of endogenous Di Methyl Histone H3 (Lys 79) (Histone H3K79me2) protein at specific gene loci using Anti- Histone H3K79me2 Recombinant Rabbit Polyclonal Antibody: Chromatin Immunoprecipitation (ChIP) was performed using Anti-Histone H3K79me2 Recombinant Rabbit Polyclonal Antibody (Product # 710802, 5 µg) on sheared chromatin from 2 million Jurkat cells using the "MAGnify ChIP system" kit (Product # 49-2024). Normal Rabbit IgG (1 µg) was used as a negative IP control. The purified DNA was analyzed by 7500 Fast qPCR system (Product # 4351106) with optimized PCR primer pairs for the promoters of the active IRF1, beta-ACTIN region used as positive control target gene, and the region of the inactive SAT2 satellite repeat, used as negative control target gene. Data is presented as fold enrichment of the antibody signal versus the negative control IgG using the comparative CT method.
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