Revision 6

#12137Store at -20C

Cell Signaling Technology

Orders: 877-616-CELL (2355) [email protected]

Support: 877-678-TECH (8324)

Web: [email protected] cellsignal.com

3 Trask LaneDanversMassachusetts01923USA
For Research Use Only. Not for Use in Diagnostic Procedures.
Applications:

WB, IP, IF-F, ChIP, ChIP-seq, C&R

REACTIVITY:

H M R

SENSITIVITY:

Endogenous

MW (kDa):

55

Source/Isotype:

Rabbit IgG

UniProt ID:

#P20265

Entrez-Gene Id:

5454

Product Information

Product Usage Information

For optimal ChIP and ChIP-seq results, use 10 μl of antibody and 10 μg of chromatin (approximately 4 x 106 cells) per IP. This antibody has been validated using SimpleChIP® Enzymatic Chromatin IP Kits.

The CUT&RUN dilution was determined using CUT&RUN Assay Kit #86652.
Application Dilution
Western Blotting 1:1000
Immunoprecipitation 1:100
Immunofluorescence (Frozen) 1:1600 - 1:3200
Chromatin IP 1:50
Chromatin IP-seq 1:50
CUT&RUN 1:50

Storage

Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/ml BSA, 50% glycerol and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody.

For a carrier free (BSA and azide free) version of this product see product #35173.

Specificity / Sensitivity

Brn2/POU3F2 (D2C1L) Rabbit mAb recognizes endogenous levels of total Brn2/POU3F2 protein.

Species Reactivity:

Human, Mouse, Rat

Source / Purification

Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues near the amino terminus of human Brn2/POU3F2 protein.

Background

Brn2/POU3F2 is a POU domain-containing transcription factor involved in neuronal differentiation and activation of the corticotrophin-releasing hormone gene (1,2). In mice, disruption of the Brn2 gene results in loss of specific neuronal lineages in the hypothalamus (3). In addition to its role in mammalian neurogenesis, Brn2 has also been implicated in melanoma tumorigenesis and has been shown in the literature to be overexpressed in human melanoma cells compared to normal melanocytes (4,5). Recent studies also identify Brn2 as a transcription factor playing an important role in keratinocyte differentiation (6). Recent reports demonstrate that overexpression of three transcription factors (Brn2, Ascl1, and Myt1L) can directly convert human fibroblasts into functional neurons under precisely defined conditions (7,8).

  1. Fujii, H. and Hamada, H. (1993) Neuron 11, 1197-206.
  2. Schonemann, M.D. et al. (1995) Genes Dev 9, 3122-35.
  3. Nakai, S. et al. (1995) Genes Dev 9, 3109-21.
  4. Cook, A.L. et al. (2003) J Invest Dermatol 121, 1150-9.
  5. Cook, A.L. and Sturm, R.A. (2008) Pigment Cell Melanoma Res 21, 611-26.
  6. Shi, G. et al. (2010) PLoS One 5, e13216.
  7. Pfisterer, U. et al. (2011) Proc Natl Acad Sci USA 108, 10343-8.
  8. Ambasudhan, R. et al. (2011) Cell Stem Cell 9, 113-8.

Species Reactivity

Species reactivity is determined by testing in at least one approved application (e.g., western blot).

Western Blot Buffer

IMPORTANT: For western blots, incubate membrane with diluted primary antibody in 5% w/v BSA, 1X TBS, 0.1% Tween® 20 at 4°C with gentle shaking, overnight.

Applications Key

WB: Western Blotting IP: Immunoprecipitation IF-F: Immunofluorescence (Frozen) ChIP: Chromatin IP ChIP-seq: Chromatin IP-seq C&R: CUT&RUN

Cross-Reactivity Key

H: human M: mouse R: rat Hm: hamster Mk: monkey Vir: virus Mi: mink C: chicken Dm: D. melanogaster X: Xenopus Z: zebrafish B: bovine Dg: dog Pg: pig Sc: S. cerevisiae Ce: C. elegans Hr: horse GP: Guinea Pig Rab: rabbit All: all species expected

Trademarks and Patents

Cell Signaling Technology is a trademark of Cell Signaling Technology, Inc.
All other trademarks are the property of their respective owners. Visit cellsignal.com/trademarks for more information.

限制使用

除非 CST 的合法授书代表以书面形式书行明确同意,否书以下条款适用于 CST、其关书方或分书商提供的书品。 任何书充本条款或与本条款不同的客书条款和条件,除非书 CST 的合法授书代表以书面形式书独接受, 否书均被拒书,并且无效。

专品专有“专供研究使用”的专专或专似的专专声明, 且未专得美国食品和专品管理局或其他外国或国内专管机专专专任何用途的批准、准专或专可。客专不得将任何专品用于任何专断或治专目的, 或以任何不符合专专声明的方式使用专品。CST 专售或专可的专品提供专作专最专用专的客专,且专用于研专用途。将专品用于专断、专防或治专目的, 或专专售(专独或作专专成)或其他商专目的而专专专品,均需要 CST 的专独专可。客专:(a) 不得专独或与其他材料专合向任何第三方出售、专可、 出借、捐专或以其他方式专专或提供任何专品,或使用专品制造任何商专专品,(b) 不得复制、修改、逆向工程、反专专、 反专专专品或以其他方式专专专专专品的基专专专或技专,或使用专品开专任何与 CST 的专品或服专专争的专品或服专, (c) 不得更改或专除专品上的任何商专、商品名称、徽专、专利或版专声明或专专,(d) 只能根据 CST 的专品专售条款和任何适用文档使用专品, (e) 专遵守客专与专品一起使用的任何第三方专品或服专的任何专可、服专条款或专似专专

Revision 6
#12137

Brn2/POU3F2 (D2C1L) Rabbit mAb

Western Blotting Image 1: Brn2/POU3F2 (D2C1L) Rabbit mAb Expand Image
使用 Brn2/POU3F2 (D2C1L) Rabbit mAb 对来自不同细胞系的提取物进行蛋白质印迹分析。
No image available
Immunofluorescence Image 1: Brn2/POU3F2 (D2C1L) Rabbit mAb Expand Image
使用 Brn2 (D7H3) Rabbit mAb(绿色)对 P1 大鼠脑进行共聚焦免疫荧光分析。使用 DY-554 phalloidin(红色)标记肌动蛋白纤丝。蓝色伪彩 = DRAQ5® #4084(DNA 荧光染料)。门区域按 10 倍放大率在右侧显示。
Chromatin Immunoprecipitation Image 1: Brn2/POU3F2 (D2C1L) Rabbit mAb Expand Image
使用 SimpleChIP® Enzymatic Chromatin IP Kit (Magnetic Beads) #9003,对 A-375 细胞中提取的交联染色质,在加入 Brn2/POU3F2 (D2C1L) Rabbit mAb #12137 后,进行染色质免疫沉淀。使用 SimpleChIP® ChIP-seq DNA Library Prep Kit for Illumina® (ChIP-seq, CUT&RUN) #56795 制备 DNA 库。本图显示整个 STRIP1 基因上的结合作用。
Chromatin Immunoprecipitation Image 2: Brn2/POU3F2 (D2C1L) Rabbit mAb Expand Image
使用 SimpleChIP® Enzymatic Chromatin IP Kit (Magnetic Beads) #9003,对 A-375 细胞中提取的交联染色质,在加入 Brn2/POU3F2 (D2C1L) Rabbit mAb 后,进行染色质免疫沉淀分析。使用 SimpleChIP® ChIP-seq DNA Library Prep Kit for Illumina® (ChIP-seq, CUT&RUN) #56795 制备 DNA 库。结果图显示在染色体 1(上图)内的接合,包括 STRIP1 基因(下图)
Chromatin Immunoprecipitation Image 3: Brn2/POU3F2 (D2C1L) Rabbit mAb Expand Image
使用 SimpleChIP® Plus Enzymatic Chromatin IP Kit (Magnetic Beads) #9005 对来自 A-375 细胞的交联染色质和 Brn2/POU3F2 (D2C1L) Rabbit mAb #12137 或 Normal Rabbit IgG #2729 进行染色质免疫沉淀分析。使用 SimpleChIP® Human MITF Promoter Primers #12377 和 SimpleChIP® Human α Satellite Repeat Primers #4486,通过实时 PCR 定量富集的 DNA。将每份样品中免疫沉淀的 DNA 的量表现为相对于所输入染色质总量(等于 1)的信号。
CUT and RUN Image 1: Brn2/POU3F2 (D2C1L) Rabbit mAb Expand Image
使用 CUT&RUN Assay Kit #86652,通过 A-375 细胞和 Brn2/POU3F2 (D2C1L) Rabbit mAb 进行 CUT&RUN 检测。‚使用 SimpleChIP® ChIP-seq DNA Library Prep Kit for Illumina® (ChIP-seq, CUT&RUN) #56795 制备 DNA 库。结果图显示在 SNRPG 内结合,SNRPG 是一种已知的 Brn2 靶标基因(参见包含 CUT&RUN-qPCR 数据的其他结果图)。
CUT and RUN Image 2: Brn2/POU3F2 (D2C1L) Rabbit mAb Expand Image
使用 CUT&RUN Assay Kit #86652,通过 A-375 细胞和 Brn2/POU3F2 (D2C1L) Rabbit mAb 进行 CUT&RUN 检测。‚使用 SimpleChIP® ChIP-seq DNA Library Prep Kit for Illumina® (ChIP-seq, CUT&RUN) #56795 制备 DNA 库。结果图显示在染色体 2(上图)内的结合,包括 Brn2 的已知靶标基因 SNRPG(下图)(参见包含 CUT&RUN-qPCR 数据的其他结果图)。
CUT and RUN Image 3: Brn2/POU3F2 (D2C1L) Rabbit mAb Expand Image
使用 CUT&RUN Assay Kit #86652,通过€‚ A-375 细胞和 Brn2/POU3F2 (D2C1L) Rabbit mAb or Rabbit (DA1E) mAb IgG XP® Isotype Control (CUT&RUN) #66362 进行 CUT&RUN。使用 human SNRPG exon 1 primers、human ATP5F1 exon 2 primers 和 SimpleChIP® Human α Satellite Repeat Primers #4486 进行实时 PCR 来对富集的 DNA 进行定量。将每份样品中免疫沉淀的 DNA 的量表现为相对于所输入染色质总量(等于 1)的信号。