merck millipore,默克密理博,17-10139,ChIPAb+™ Phospho-Histone H3 (Thr11)

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merck millipore,默克密理博,17-10139,ChIPAb+™ Phospho-Histone H3 (Thr11) - ChIP Validated Antibody and Primer Set
产品名称：ChIPAb+™ Phospho-Histone H3 (Thr11) - ChIP Validated Antibody and Primer Set
产品型号：17-10139
This ChIPAb+ Phospho-Histone H3 (Thr11) -ChIP Validated Antibody & Primer Set conveniently includes the antibody & the specific control PCR primers.

merck millipore,默克密理博,17-10139,ChIPAb+™ Phospho-Histone H3 (Thr11) - ChIP Validated Antibody and Primer Set

产品介绍

merck millipore,默克密理博,17-10139,ChIPAb+™ Phospho-Histone H3 (Thr11) - ChIP Validated Antibody and Primer Set

重要规格表

品种反应性	主要应用
Vrt, H	WB, ChIP

描述
产品目录编号	17-10139
商名	Upstate ChIPAb+
描述	ChIPAb+™ Phospho-Histone H3 (Thr11) - ChIP Validated Antibody and Primer Set
概述	All ChIPAb+ antibodies are individually validated for chromatin precipitation, every lot, every time. Each ChIPAb+ antibody set includes control primers (tested every lot by qPCR) to biologically validate your IP results in a locus-specific context. The qPCR protocol and primer sequences are provided, allowing researchers to validate ChIP protocols when using our antibody in their chromatin context. Each set also includes a negative control antibody to ensure specificity of the ChIP reaction. The ChIPAb+ Phospho-Histone H3 (Thr11) set includes the Phospho-Histone H3 (Thr11) antibody, a Normal rabbit IgG, and control primers which amplify a 166 bp region of human GAPDH promoter. The Phospho-Histone H3 (Thr11) and negative controls are supplied in a scalable "per ChIP" reaction size and can be used to functionally validate the precipitation of Phospho-Histone H3 (Thr11) -associated chromatin.
Alternate Names	Histone H3 (phospho T11) H3T11P
背景信息	Histone H3 is one of the five main histone proteins involved in the structure of chromatin in eukaryotic cells. Featuring a main globular domain and a long N-terminal tail, H3 is involved with the structure of the nucleosomes of the 'beads on a string' structure. The N-terminal tail of histone H3 protrudes from the globular nucleosome core and can undergo several different types of epigenetic modifications 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.

产品信息
格式	Affinity Purified
控制	Includes normal rabbit IgG and primers specific for human GAPDH promoter.
演示	Anti-Phospho-Histone H3 (Thr11) (rabbit polyclonal), . One vial containing 25 µL of rabbit antiserum depleted of non-phospho-histone H3 specific antibodies and 0.05% sodium azide before the addition of 30% gycerol. Store at -20°C. Normal Rabbit IgG. One vial containing 125 µg of Rabbit IgG in 125 µL of storage buffer containing 0.05% sodium azide. Store at -20°C. Control Primers, human GAPDH promoter. One vial containing 75 μL of 5 μM of each primer specific for human GAPDH. Store at -20°C. FOR: TAC TAG CGG TTT TAC GGG CG REV: TCG AAC AGG AGG AGC AGA GAG CGA

应用
应用	This ChIPAb+ Phospho-Histone H3 (Thr11) -ChIP Validated Antibody & Primer Set conveniently includes the antibody & the specific control PCR primers.
主要应用	Western Blotting Chromatin Immunoprecipitation (ChIP)
应用说明	Chromatin Immunoprecipitation: Representative lot data. Sonicated chromatin prepared from untreated or colcemid-treated HeLa cells (1 X 10E6 cell equivalents per IP) were subjected to chromatin immunoprecipitation using either 1 µL of normal rabbit IgG or 1 µL of Anti-Phospho-Histone H3 (Thr11) and the Magna ChIP™ A Kit (Cat. # 17-610). Successful immunoprecipitation of Phospho-Histone H3 (Thr11) associated DNA fragments was verified by qPCR using ChIP Primers, human GAPDH promoter Region for untreated and treated chromatin samples . Data is presented as percent input of each IP sample relative to input chromatin for each amplicon and ChIP sample as indicated. Please refer to the EZ-Magna ChIP™ A (Cat. # 17-408) or EZ-ChIP™ (Cat. # 17-371) protocol for experimental details. Western Blot Analysis: Representative lot data. 20 micrograms of acid-extracted proteins from untreated (lane1) or colcemid treated (lane 2) HeLa cells were probed with Anti-Phospho-Histone H3 (Thr 11) (1:20,000 dilution). Arrow indicates Phospho-Histone H3 (Thr 11). Beadlyte® Histone-Peptide Specificity Assay: Representative lot data. 1:4,000-1:16,000 of this lot was incubated with a cocktail of microspheres conjugated to Histone H3 peptides with the following modifications: 1. no modifications 2. phosphothreonine 3 3. phosphoserine 10 4. phosphothreonine 11 5. phosphothreonine 22 Unbound antibody was then removed by filtration. Peptide-antibody complexes were incubated with a biotin-conjugated anti-rabbit secondary antibody followed by incubation with a phycoerythrinstreptavidin conjugate. Fluorescence was read on a Luminex® 100™ instrument. Median Fluorescence Intensity (MFI) is plotted.

生物信息
免疫原品种	Peptide containing (KS[pT]GG), in which pT corresponds to phosphothreonine 11 of human histone H3.
表位	Phosphorylated Thr11
宿主	Rabbit
特异性	histone H3 phosphorylated at threonine 11
品种反应性	VertebratesHuman
抗体类型	Polyclonal Antibody
Entrez基因编号	NM_003493
Entrez基因汇总	Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a member of the histone H3 family. Transcripts from this gene lack polyA tails; instead, they contain a palindromic termination element. This gene is located separately from the other H3 genes that are in the histone gene cluster on chromosome 6p22-p21.3.
基因符号	MGC126886 HIST3H3 H3FT H3/t H3t MGC126888 H3/g H3.4 H3T
修改	Phosphorylation
纯化方法	Antiserum
UniProt编号	Q16695
UniProt汇总	FUNCTION: SwissProt: Q16695 # Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling. SIZE: 136 amino acids; 15508 Da SUBUNIT: The nucleosome is a histone octamer containing two molecules each of H2A, H2B, H3 and H4 assembled in one H3-H4 heterotetramer and two H2A-H2B heterodimers. The octamer wraps approximately 147 bp of DNA. SUBCELLULAR LOCATION: Nucleus. TISSUE SPECIFICITY: Expressed in testicular cells. DEVELOPMENTAL STAGE: Expressed during S phase, then expression strongly decreases as cell division slows down during the process of differentiation. PTM: Acetylation is generally linked to gene activation. Acetylation on Lys-10 impairs methylation at Arg-9. Acetylation on Lys-19 and Lys-24 favors methylation at Arg-18 (By similarity). & Citrullination at Arg-9 and/or Arg-18 by PADI4 impairs methylation and represses transcription (By similarity). & Asymmetric dimethylation at Arg-18 by CARM1 is linked to gene activation. Symmetric dimethylation at Arg-9 by PRMT5 is linked to gene repression (By similarity). & Methylation at Lys-5, Lys-37 and Lys-80 are linked to gene activation. Methylation at Lys-5 facilitates subsequent acetylation of H3 and H4. Methylation at Lys-80 is associated with DNA double-strand break (DSB) responses and is a specific target for TP53BP1. Methylation at Lys-10 and Lys-28 are linked to gene repression. Methylation at Lys-10 is a specific target for HP1 proteins (CBX1, CBX3 and CBX5) and prevents subsequent phosphorylation at Ser-11 and acetylation of H3 and H4. Methylation at Lys-5 and Lys-80 require preliminary monoubiquitination of H2B at 'Lys-120'. Methylation at Lys-10 and Lys-28 are enriched in inactive X chromosome chromatin (By similarity). & Phosphorylated at Thr-4 by GSG2/haspin during prophase and dephosphorylated during anaphase. At centromeres, specifically phosphorylated at Thr-12 from prophase to early anaphase. Phosphorylated at Ser-11 during the whole mitosis. Phosphorylation at Ser-11, which is linked to gene activation, prevents methylation at Lys-10 but facilitates acetylation of H3 and H4. Phosphorylated at Ser-29 by MLTK isoform 1, RPS6KA5 or AURKB during mitosis or upon ultraviolet B irradiation (By similarity). & Phosphorylation at 'Ser-11' is crucial for chromosome condensation and cell-cycle progression during mitosis and meiosis. In addition phosphorylation at 'Ser-11' is important during interphase because it enables the transcription of genes following external stimulation, like stress or growth factors. Phosphorylation at 'Ser-11' is also an essential regulatory mechanism for neoplastic cell transformation. Phosphorylation at 'Ser-11' by AURKB/Aurora-B mediates the dissociation of HP1 proteins (CBX1, CBX3 and CBX5) from heterochromatin. & Ubiquitinated (By similarity). SIMILARITY: SwissProt: Q16695 ## Belongs to the histone H3 family.

产品使用声明
质量保证	Chromatin Immunoprecipitation: Representative lot data. Sonicated chromatin prepared from colcemid-treated HeLa cells (1 X 10E6 cell equivalents per IP) were subjected to chromatin immunoprecipitation using either 1 µL of normal rabbit IgG or 1 µL of Anti-phospho-Histone H3 (Thr11) and the Magna ChIP™ A Kit (Cat. # 17-610). Successful immunoprecipitation of phospho-Histone H3 (Thr11) associated DNA fragments was verified by qPCR using ChIP Primers, human GAPDH promoter Region. Please refer to the EZ-Magna ChIP™ A (Cat. # 17-408) or EZ-ChIP™ (Cat. # 17-371) protocol for experimental details.
使用声明	Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

产品使用声明

质量保证

Chromatin Immunoprecipitation:
Representative lot data.
Sonicated chromatin prepared from colcemid-treated HeLa cells (1 X 10E6 cell equivalents per IP) were subjected to chromatin immunoprecipitation using either 1 µL of normal rabbit IgG or 1 µL of Anti-phospho-Histone H3 (Thr11) and the Magna ChIP™ A Kit (Cat. # 17-610). Successful immunoprecipitation of phospho-Histone H3 (Thr11) associated DNA fragments was verified by qPCR using ChIP Primers, human GAPDH promoter Region.
Please refer to the EZ-Magna ChIP™ A (Cat. # 17-408) or EZ-ChIP™ (Cat. # 17-371) protocol for experimental details.

使用声明

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

储存和货运信息
存储条件	Stable for 1 year at -20°C from date of receipt. Handling Recommendations: Upon first thaw, and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance. Note: Variability in freezer temperatures below -20°C may cause glycerol containing solutions to become frozen during storage.

储存和货运信息

存储条件

Stable for 1 year at -20°C from date of receipt. Handling Recommendations: Upon first thaw, and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.
Note: Variability in freezer temperatures below -20°C may cause glycerol containing solutions to become frozen during storage.