Revision 6

#12972Store 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, IHC-P, IF-IC, FC-FP, ChIP, ChIP-seq, C&R

REACTIVITY:

H M R Mk B Dg Pg

SENSITIVITY:

Endogenous

MW (kDa):

80

Source/Isotype:

Rabbit IgG

UniProt ID:

#Q00613

Entrez-Gene Id:

3297

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 1:50
Immunohistochemistry (Paraffin) 1:250 - 1:1000
Immunofluorescence (Immunocytochemistry) 1:200 - 1:400
Flow Cytometry (Fixed/Permeabilized) 1:100 - 1:400
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 #76196.

Specificity / Sensitivity

HSF1 (D3L8I) Rabbit mAb recognizes endogenous levels of total HSF1 protein. This antibody is not predicted to cross-react with HSF2.

Species Reactivity:

Human, Mouse, Rat, Monkey, Bovine, Dog, Pig

Source / Purification

Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues near the carboxy terminus of human HSF1 protein.

Background

All organisms respond to increased temperatures and other environmental stresses by rapidly inducing the expression of highly conserved heat shock proteins (HSPs) that serve as molecular chaperones to refold denatured proteins and promote the degradation of damaged proteins. Heat shock gene transcription is regulated by a family of heat shock factors (HSFs), transcriptional activators that bind to heat shock response elements (HSEs) located upstream of all heat shock genes (1). HSEs are highly conserved among organisms and contain multiple adjacent and inverse iterations of the pentanucleotide motif 5'-nGAAn-3'. HSFs are less conserved and share only 40% sequence identity. Vertebrate cells contain four HSF proteins: HSF1, 2 and 4 are ubiquitous, while HSF3 has only been characterized in avian species. HSF1 induces heat shock gene transcription in response to heat, heavy metals, and oxidative agents, while HSF2 is involved in spermatogenesis and erythroid cell development. HSF3 and HSF4 show overlapping functions with HSF1 and HSF2. The inactive form of HSF1 exists as a monomer that localizes to both the cytoplasm and nucleus, but does not bind DNA (1,2). In response to stress, HSF1 becomes phosphorylated, forms homotrimers, binds DNA and activates heat shock gene transcription (1,2). HSF1 activity is positively regulated by phosphorylation of Ser419 by PLK1, which enhances nuclear translocation, and phosphorylation of Ser230 by CaMKII, which enhances transactivation (3,4). Alternatively, HSF1 activity is repressed by phosphorylation of serines at 303 and 307 by GSK3 and ERK1, respectively, which leads to binding of 14-3-3 protein and sequestration of HSF1 in the cytoplasm (5,6). In addition, during attenuation from the heat shock response, HSF1 is repressed by direct binding of Hsp70, HSP40/Hdj-1, and HSF binding protein 1 (HSBP1) (7).

  1. Morimoto, R.I. (1998) Genes Dev 12, 3788-96.
  2. Mercier, P.A. et al. (1999) J Cell Sci 112 ( Pt 16), 2765-74.
  3. Kim, S.A. et al. (2005) J Biol Chem 280, 12653-7.
  4. Holmberg, C.I. et al. (2001) EMBO J 20, 3800-10.
  5. Chu, B. et al. (1996) J Biol Chem 271, 30847-57.
  6. Wang, X. et al. (2003) Mol Cell Biol 23, 6013-26.
  7. Satyal, S.H. et al. (1998) Genes Dev 12, 1962-74.

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 IHC-P: Immunohistochemistry (Paraffin) IF-IC: Immunofluorescence (Immunocytochemistry) FC-FP: Flow Cytometry (Fixed/Permeabilized) 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.
Alexa Fluor is a registered trademark of Life Technologies Corporation.
The transfer of the secondary cocktail contained in this kit is contingent on the buyer using the purchased product solely in research conducted by the buyer (whether the buyer is an academic or for-profit entity), for immunocytochemistry, high content screening (HCS) analysis, or flow cytometry applications. The sale of this product is expressly conditioned on the buyer not using the product or its components (1) in manufacturing; (2) to provide a service, information, or data to an unaffiliated third party for payment; (3) for therapeutic, diagnostic or prophylactic purposes; (4) resale, whether or not such product or its components are resold for use in research; or for any other commercial purpose. For information on purchasing a license to this product for purposes other than research, contact Life Technologies Corporation, 5791 Van Allen Way, Carlsbad, CA 92008 USA or [email protected]. Alexa Fluor® is a registered trademark of Molecular Probes, 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
#12972

HSF1 (D3L8I) Rabbit mAb

Western Blotting Image 1: HSF1 (D3L8I) Rabbit mAb Expand Image
使用 HSF1 (D3L8I) Rabbit mAb 对不同细胞系提取物进行蛋白质印迹分析。
Immunoprecipitation Image 1: HSF1 (D3L8I) Rabbit mAb Expand Image
使用 Rabbit (DA1E) mAb IgG XP® Isotype Control #3900(泳道 2)、HSF1 Antibody #4356(泳道 3)或 HSF1 (D8L8I) Rabbit mAb(泳道 4),对 HeLa 细胞提取物 HSF1 进行免疫沉淀。泳道 1 是 10% 输入对照。使用 HSF1 (D8L8I) Rabbit mAb 进行蛋白质印迹分析。
Immunohistochemistry Image 1: HSF1 (D3L8I) Rabbit mAb Expand Image
使用 HSF1 (D3L8I) Rabbit mAb 对石蜡包埋的人肺癌进行免疫组织化学分析。
Immunohistochemistry Image 2: HSF1 (D3L8I) Rabbit mAb Expand Image
在对照肽(左)或抗原特异性肽(右)存在的情况下,使用 HSF1 (D3L8I) Rabbit mAb 对石蜡包埋的人结肠癌进行免疫组织化学分析。
Immunohistochemistry Image 3: HSF1 (D3L8I) Rabbit mAb Expand Image
使用 HSF1 (D3L8I) Rabbit mAb 对石蜡包埋的人前列腺癌进行免疫组织化学分析。
Immunohistochemistry Image 4: HSF1 (D3L8I) Rabbit mAb Expand Image
使用 HSF1 (D3L8I) Rabbit mAb 对石蜡包埋的 HSF1 野生型(左)、HSF1 敲除型(中)或 HSF2 敲除型(右)的小鼠脾脏进行免疫组织化学分析。组织由 Georgia Health Sciences University, Atlanta, Georgia 的 Nahid Mivechi 博士惠赠。
Immunofluorescence Image 1: HSF1 (D3L8I) Rabbit mAb Expand Image
使用 HSF1 (D3L8I) Rabbit mAb(绿色),对未经处理或经热处理(43.5ºC,1 小时,不恢复)的 HeLa 细胞进行共聚焦免疫荧光分析。肌动蛋白丝用 DyLight® 554 Phalloidin #13054(红色)标记。热休克后,HSF1 被重新分配到细胞核应激颗粒中(见插图)。
Flow Cytometry Image 1: HSF1 (D3L8I) Rabbit mAb Expand Image
以浓度匹配的 Rabbit (DA1E) mAb IgG XP® Isotype Control #3900(虚线)作为对照,使用 HSF1 (D3L8I) Rabbit mAb(实线)对 HeLa 细胞进行流式细胞分析。Anti-rabbit IgG (H+L)、F(ab')2 Fragment (Alexa Fluor® 488 Conjugate) #4412 作为二抗。
Chromatin Immunoprecipitation Image 1: HSF1 (D3L8I) Rabbit mAb Expand Image
使用 SimpleChIP® 酶解染色质免疫共沉淀试剂盒(磁珠法) #9005 对热休克 1 小时的 HeLa 细胞的交联染色质与 HSF1 (D3L8I) 兔单克隆抗体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。该结果图显示在 HSF1 的一个已知靶基因 HSPA6 内结合(参见包含 ChIP-qPCR 数据的其他结果图)。
Chromatin Immunoprecipitation Image 2: HSF1 (D3L8I) Rabbit mAb Expand Image
使用 SimpleChIP® 酶解染色质免疫共沉淀试剂盒(磁珠法) #9005 对热休克 1 小时的 HeLa 细胞的交联染色质与 HSF1 (D3L8I) 兔单克隆抗体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。结果图显示在染色体(上图)内的结合,包括 HSF1 的已知靶标基因 HSPA6(下图)(参见包含 ChIP-qPCR 数据的其他结果图)。
Chromatin Immunoprecipitation Image 3: HSF1 (D3L8I) Rabbit mAb Expand Image
使用 SimpleChIP® Enzymatic Chromatin IP Kit (Magnetic Beads) #9003,对热休克 1 小时的HeLa 细胞的交联染色质、HSF1 (D3L8I) Rabbit mAb 或 Normal Rabbit IgG #2729 进行染色质免疫沉淀。使用 SimpleChIP® Human HSPA6 Promoter Primers #5551、Human HSP70 Intron 1 Primers 和 SimpleChIP® Human α Satellite Repeat Primers #4486 并通过实时 PCR 对富集的 DNA 进行定量分析。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: HSF1 (D3L8I) Rabbit mAb Expand Image
使用 CUT&RUN 检测试剂盒 #86652,对热激 1 小时的 HeLa 细胞和 HSF1 (D3L8I) 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 HSP90AB1 基因内结合。
CUT and RUN Image 2: HSF1 (D3L8I) Rabbit mAb Expand Image
使用 CUT&RUN 检测试剂盒 #86652,对热激 1 小时的 HeLa 细胞和 HSF1 (D3L8I) 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 6(上图)内的结合,包括 HSP90AB1 基因(下图)。
CUT and RUN Image 3: HSF1 (D3L8I) Rabbit mAb Expand Image
使用 CUT&RUN Assay Kit #86652,对热休克 1 小时的 HeLa 细胞和 HSF1 (D3L8I) Rabbit mAb 或 Rabbit (DA1E) mAb IgG XP® Isotype Control (CUT&RUN) #66362 进行 CUT&RUN 检测。使用人 CRTC2 内含子 1 引物和人 ITM2A 上游引物通过实时 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。