Anti-Cyclin D1 antibody [SP4]

• 产品名称

  Anti-Cyclin D1抗体[SP4]
  参阅全部 Cyclin D1 一抗

• 描述

  兔单克隆抗体[SP4] to Cyclin D1

• 宿主

  Rabbit

• 经测试应用

  适用于: ICC/IF, Flow Cyt (Intra), WB, IHC-Pmore details

• 种属反应性

  与反应: Mouse, Rat, Human
  

• 免疫原

  Synthetic peptide. This information is considered to be commercially sensitive.

• 表位

  C-terminus

• 阳性对照

• WB: MCF7, Hap1, A431 and HeLa, Nuero-2a, NIH/3T3, C6, Wild-type A549 and SH-SY5Y cell lysates. IHC (FFPE): Human normal tonsil; breast carcinoma; mantle cell lymphoma; rat esophagus. ICC/IF: MCF7 cells, C6, Neuro-2a and HAP1 cells (HAP1-CCND1 knockout cells used as negative cell line). Flow Cyt (intra): MCF7, NIH/3T3 and C6 cells.

• 常规说明

  This product was switched from a hybridoma to recombinant production method on 22nd January 2019.

  This product is a recombinant monoclonal antibody, which offers several advantages including:

  For more information see here.

  Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.

  
  

  This product is FOR RESEARCH USE ONLY. For commercial use, please contact partnerships@abcam.com.

• - High batch-to-batch consistency and reproducibility

• - Improved sensitivity and specificity

• - Long-term security of supply

• - Animal-free production

• 形式

  Liquid

• 存放说明

  Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid repeated freeze / thaw cycles.

• 存储溶液

  pH: 7.20
  Preservative: 0.1% Sodium azide
  Constituents: 1% BSA, PBS

• 浓度

• 批次浓度范围 100 µl 浓度为 0.045 - 0.053 mg/ml

• 批次浓度范围 1 ml 浓度为 0.045 - 0.053 mg/ml

• 批次浓度范围 500 µl 浓度为 0.045 - 0.053 mg/ml

• 纯度

  Protein A purified

• 克隆

  单克隆

• 克隆编号

  SP4

• 同种型

  IgG

The Abpromise guarantee

Abpromise™承诺保证使用ab16663于以下的经测试应用

“应用说明”部分 下显示的仅为推荐的起始稀释度；实际最佳的稀释度/浓度应由使用者检定。

• 数据库链接

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• Unigene: 667996 Human

• Unigene: 273049 Mouse

• Unigene: 22279 Rat

• Entrez Gene: 595 Human

• Entrez Gene: 12443 Mouse

• Entrez Gene: 58919 Rat

• Omim: 168461 Human

• SwissProt: P24385 Human

• SwissProt: P25322 Mouse

• SwissProt: P39948 Rat

• Unigene: 523852 Human

• 别名

• B cell lymphoma 1 protein antibody

• B-cell lymphoma 1 protein antibody

• BCL 1 antibody

• BCL-1 antibody

• BCL-1 oncogene antibody

• BCL1 antibody

• BCL1 oncogene antibody

• ccnd1 antibody

• CCND1/FSTL3 fusion gene antibody

• CCND1/FSTL3 fusion gene, included antibody

• CCND1/IGHG1 fusion gene antibody

• CCND1/IGHG1 fusion gene, included antibody

• CCND1/IGLC1 fusion gene antibody

• CCND1/IGLC1 fusion gene, included antibody

• CCND1/PTH fusion gene antibody

• CCND1/PTH fusion gene, included antibody

• CCND1_HUMAN antibody

• cD1 antibody

• Cyl 1 antibody

• D11S287E antibody

• G1/S specific cyclin D1 antibody

• G1/S-specific cyclin-D1 antibody

• Parathyroid adenomatosis 1 antibody

• PRAD1 antibody

• PRAD1 oncogene antibody

• U21B31 antibody

• AI327039 antibody

• B cell CLL/lymphoma 1 antibody

• B cell leukemia 1 antibody

• 

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Cyclin D1 antibody [SP4] (ab16663)

  Immunohistochemical analysis of formalin fixed paraffin embedded human tonsil labelling CyclinD1 with ab16663 at a dilution of 1/200.

  The immunostaining was performed on a Ventana DISCOVERY ULTRA (Roche Tissue Diagnostics) instrument with an OptiView DAB IHC Detection Kit. Heat mediated antigen retrieval was conducted for 32min with DISCOVERY cell conditioning solution (CC1) 100°C, pH8.5. ab16663 CyclinD1 was incubated at 37°C for 16min.

  Sections were counterstained is with Hematoxylin II. Image inset shows absence of staining in secondary antibody only control.

  Customers are encouraged to optimise antigen retrieval conditions, antibody concentration, incubation times and temperature for best results in their own IHC assay workflow (automated and manual)

• 

  Western blot - Anti-Cyclin D1 antibody [SP4] (ab16663)

  All lanes : Anti-Cyclin D1 antibody [SP4] (ab16663) at 1/25 dilution
  
  Lane 1 : Wild-type A549 cell lysate
  Lane 2 : ccnd1 knockout A549 cell lysate
  Lane 3 : SH-SY5Y cell lysate
  Lane 4 : K562 cell lysate
  
  Lysates/proteins at 20 µg per lane.
  
  Secondary
  All lanes : Goat anti-Rabbit IgG H&L 800CW and Goat anti-Mouse IgG H&L 680RD at 1/20000 dilution
  
  Performed under reducing conditions.
  
  Predicted band size: 33 kDa
  Observed band size: 35 kDawhy is the actual band size different from the predicted?
  
  
  
  

  False colour image of Western blot: Anti-Cyclin D1 antibody [SP4] staining at 1/25 dilution, shown in green; Mouse anti-Alpha Tubulin [DM1A] (ab7291) loading control staining at 1/20000 dilution, shown in red. In Western blot, ab16663 was shown to bind specifically to Cyclin D1. A band was observed at 35 kDa in wild-type A549 cell lysates with no signal observed at this size in ccnd1 knockout cell line ab286759 (knockout cell lysate ab300213). To generate this image, wild-type and ccnd1 knockout A549 cell lysates were analysed. First, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 3 % milk in TBS-0.1 % Tween® 20 (TBS-T) before incubation with primary antibodies overnight at 4 °C. Blots were washed four times in TBS-T, incubated with secondary antibodies for 1 h at room temperature, washed again four times then imaged. Secondary antibodies used were Goat anti-Rabbit IgG H&L 800CW and Goat anti-Mouse IgG H&L 680RD at 1/20000 dilution.

• 

  Western blot - Anti-Cyclin D1 antibody [SP4] (ab16663)

  All lanes : Anti-Cyclin D1 antibody [SP4] (ab16663) at 1/200 dilution
  
  Lane 1 : Wild-type HeLa cell lysate
  Lane 2 : CCND1 knockout HeLa cell lysate
  
  Lysates/proteins at 20 µg per lane.
  
  Performed under reducing conditions.
  
  Predicted band size: 33 kDa
  Observed band size: 36 kDawhy is the actual band size different from the predicted?
  
  
  
  

  Lanes 1- 2: Merged signal (red and green). Green - ab16663 observed at 36 kDa. Red - Anti-Vinculin antibody [VIN-54] observed at 124 kDa.

   ab16663 was shown to react with CCND1 in wild-type HeLa cells in western blot. Loss of signal was observed when knockout cell line ab255348 (knockout cell lysate ab263808) was used. Wild-type HeLa and CCND1 knockout HeLa cell lysates were subjected to SDS-PAGE. Membrane was blocked for 1 hour at room temperature in 0.1% TBST with 3% non-fat dried milk. ab16663 and Anti-Vinculin antibody [VIN-54] overnight at 4°C at a 1 in 200 dilution and a 1 in 20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye®800CW) preadsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye®680RD) preadsorbed (ab216776) secondary antibodies at 1 in 20000 dilution for 1 hour at room temperature before imaging.

• 

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Cyclin D1 antibody [SP4] (ab16663)

  IHC image of ab16663 staining Cyclin D1 in a section of formalin-fixed paraffin-embedded normal human tonsil* performed on a Leica BONDTM system using the standard protocol F. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20mins. The section was then incubated with ab16663, 1/100 dilution, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre

  This image was generated from the hybridoma version.

   

• 

  Western blot - Anti-Cyclin D1 antibody [SP4] (ab16663)

  Anti-Cyclin D1 antibody [SP4] (ab16663) at 1/200 dilution + Wild-type HeLa cell lysate at 20 µg
  
  Performed under reducing conditions.
  
  Predicted band size: 33 kDa
  Observed band size: 36 kDawhy is the actual band size different from the predicted?
  
  
  
  

  Lanes 1- 2: Merged signal (red and green). Green - ab16663 observed at 36 kDa. Red - Anti-alpha Tubulin antibody [DM1A] - Loading Control (ab7291) observed at 50 kDa.

   ab16663 was shown to react with Cyclin D1 in wild-type HeLa cells in western blot. Loss of signal was observed when knockout cell line ab261760 (knockout cell lysate ab256864) was used. Wild-type HeLa and CCND1 knockout HeLa cell lysates were subjected to SDS-PAGE. Membrane was blocked for 1 hour at room temperature in 0.1% TBST with 3% non-fat dried milk. ab16663 and Anti-alpha Tubulin antibody [DM1A] - Loading Control (ab7291) overnight at 4°C at a 1 in 200 dilution and a 1 in 20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye®800CW) preadsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye®680RD) preadsorbed (ab216776) secondary antibodies at 1 in 20000 dilution for 1 hour at room temperature before imaging.

• 

  Immunocytochemistry/ Immunofluorescence - Anti-Cyclin D1 antibody [SP4] (ab16663)

  Immunocytochemistry/ Immunofluorescence analysis of C6 (rat glial tumor glial cell) cells labeling Cyclin D1 with purified ab16663 at 1/50 (5.42µg/ml). Cells were fixed in 4% paraformaldehyde and permeabilized with 0.1% Triton X-100. Cells were counterstained with ab195889 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) 1/200 (2.5 µg/ml). Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) was used as the secondary antibody at 1/1000 (2 µg/ml) dilution. DAPI was used as nuclear counterstain. PBS instead of the primary antibody was used as the secondary antibody only control.

  This image was generated from the hybridoma version.

   

• 

  Flow Cytometry (Intracellular) - Anti-Cyclin D1 antibody [SP4] (ab16663)

  Intracellular flow cytometry analysis of MCF-7 (human breast carcinoma) labeling Cyclin D1 with purified ab16663 at 1/30 dilution (9.03 µg/ml) (red). Cells were fixed with 4% paraformaldehyde and permeabilised with 90% methanol. Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) at 1/2000 dilution was used as a secondary antibody. Isotype control - Rabbit monoclonal IgG (ab172730) (Black). Unlableled control - Unlabelled cells (blue). This image was generated from the hybridoma version.

• 

  Western blot - Anti-Cyclin D1 antibody [SP4] (ab16663)

  All lanes : Anti-Cyclin D1 antibody [SP4] (ab16663) at 1/1000 dilution
  
  Lane 1 : HeLa (Human cervix adenocarcinoma epithelial cell) cell lysate
  Lane 2 : MCF7 (Human breast adenocarcinoma epithelial cell) cell lysate
  Lane 3 : CCND1 KO HAP1 cell lysate
  Lane 4 : HAP1 (Human chronic myelogenous leukemia near-haploid cell line) cell lysate
  Lane 5 : Neuro-2a (Mouse neuroblastoma neuroblast) cell lysate
  Lane 6 : NIH/3T3 (Mouse embryonic fibroblast) cell lysate
  Lane 7 : C6 (Rat glial tumor glial cell) cell lysate
  
  Lysates/proteins at 10 µg per lane.
  
  Secondary
  All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/20000 dilution
  
  Predicted band size: 33 kDa
  Observed band size: 33 kDa
  
  
  Exposure time: 2 seconds
  

• 

  Western blot - Anti-Cyclin D1 antibody [SP4] (ab16663)

  All lanes : Anti-Cyclin D1 antibody [SP4] (ab16663)
  
  Lane 1 : Wild-type HAP1 whole cell lysate
  Lane 2 : CCND1 (Cyclin D1) knockout HAP1 whole cell lysate
  Lane 3 : A431 whole cell lysate
  
  Lysates/proteins at 20 µg per lane.
  
  Predicted band size: 33 kDa
  
  
  
  

  Lanes 1 - 3: Merged signal (red and green). Green - ab16663 observed at 34 kDa. Red - loading control, ab18058, observed at 130 kDa.

  ab16663 was shown to specifically recognize CCND1 (Cyclin D1) in wild-type HAP1 cells as signal was lost at the expected MW in CCND1 (Cyclin D1) knockout cells. Wild-type and CCND1 (Cyclin D1) knockout samples were subjected to SDS-PAGE. Ab16663 and ab18058 (Mouse anti Vinculin loading control) were incubated overnight at 4°C at 1/200 dilution and 1/20,000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed (ab216776) secondary antibodies at 1/20,000 dilution for 1 hour at room temperature before imaging.

  This image was generated from the hybridoma version.

   

• 

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Cyclin D1 antibody [SP4] (ab16663)

  IHC image of ab16663 staining Cyclin D1 in rat esophagus formalin fixed paraffin embedded tissue sections, performed on a Leica Bond. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20 mins. The section was then incubated with ab16663, 1:100 dilution, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. No primary antibody was used in the secondary only control (shown on the inset).
  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  This image was generated from the hybridoma version.

   

• 

  Immunocytochemistry/ Immunofluorescence - Anti-Cyclin D1 antibody [SP4] (ab16663)

  Immunocytochemistry/ Immunofluorescence analysis of Neuro-2a (mouse neuroblastoma neuroblast) cells labeling Cyclin D1µ with purified ab16663 at 1/50 (5.42µg/ml). Cells were fixed in 4% paraformaldehyde and permeabilized with 0.1% Triton X-100. Cells were counterstained with ab195889 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) 1/200 (2.5 µg/ml). Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) was used as the secondary antibody at 1/1000 (2 µg/ml) dilution. DAPI was used as nuclear counterstain. PBS instead of the primary antibody was used as the secondary antibody only control.

  This image was generated from the hybridoma version.

   

• 

  Immunocytochemistry/ Immunofluorescence - Anti-Cyclin D1 antibody [SP4] (ab16663)

  ab16663 staining Cyclin D1 in MCF7 cells. The cells were fixed with 4% formaldehyde (10 min), permeabilized in 0.1% Triton X-100 for 5 minutes and then blocked in 1% BSA/10% normal goat serum/0.3M glycine in 0.1% PBS-Tween for 1h. The cells were then incubated with ab16663 at a working dilution of 1/250 and ab195889, Mouse monoclonal [DM1A] to alpha Tubulin (Alexa Fluor® 594, shown in red) at 1/250 overnight at +4°C, followed by a further incubation at room temperature for 1h with an anti-rabbit AlexaFluor® 488 (ab150081) at 2 μg/ml (shown in green). Nuclear DNA was labelled in blue with DAPI.
  Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).

  This image was generated from the hybridoma version.

   

• 

  Flow Cytometry (Intracellular) - Anti-Cyclin D1 antibody [SP4] (ab16663)

  Intracellular flow cytometry analysis of C6 (rat glioma) labeling Cyclin D1 with purified ab16663 at 1/30 dilution (9.03 µg/ml) (red). Cells were fixed with 4% paraformaldehyde and permeabilised with 90% methanol. Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) at 1/2000 dilution was used as a secondary antibody. Isotype control - Rabbit monoclonal IgG (ab172730) (Black). Unlableled control - Unlabelled cells (blue). This image was generated from the hybridoma version.

• 

  Flow Cytometry (Intracellular) - Anti-Cyclin D1 antibody [SP4] (ab16663)

  Intracellular flow cytometry analysis of NIH/3T3 (mouse embryo) labeling Cyclin D1 with purified ab16663 at 1/30 dilution (9.03 µg/ml) (red). Cells were fixed with 4% paraformaldehyde and permeabilised with 90% methanol. Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) at 1/2000 dilution was used as a secondary antibody. Isotype control - Rabbit monoclonal IgG (ab172730) (Black). Unlableled control - Unlabelled cells (blue).  This image was generated from the hybridoma version.

   

• 

  Immunocytochemistry/ Immunofluorescence - Anti-Cyclin D1 antibody [SP4] (ab16663)

  ab16663 staining Cyclin D1 in wild-type HAP1 cells (top panel) and CCND1 knockout HAP1 cells (bottom panel). The cells were fixed with 100% methanol (5min), permeabilized with 0.1% Triton X-100 for 5 minutes and then blocked with 1% BSA/10% normal goat serum/0.3M glycine in 0.1% PBS-Tween for 1h. The cells were then incubated with ab16663 at 1/250 dilution and ab195889 at 1/250 dilution (shown in pseudocolour red) overnight at +4°C, followed by a further incubation at room temperature for 1h with a goat secondary antibody to Rabbit IgG (Alexa Fluor® 488) (ab150081) at 2 μg/ml (shown in green). Nuclear DNA was labelled in blue with DAPI.

  Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).

  This image was generated from the hybridoma version.

   

• 

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Cyclin D1 antibody [SP4] (ab16663)Image from McIver SC et al., PLoS One. 2012;7(4):e35553. Epub 2012 Apr 20. Fig 7.; doi:10.1371/journal.pone.0035553; April 20, 2012, PLoS ONE 7(4): e35553.

  Immunohistochemical analysis of mouse testis tissue, staining Cyclin D1 with ab16663.
  
  Antigen retrieval was performed via Tris-EDTA buffer. Sections were blocked with 3% BSA and incubated with primary antibody (1/50) overnight at 4°C. An AlexaFluor®594-conjugated secondary antibody was used to detect staining.

  This image was generated from the hybridoma version.

   

• 

  Western blot - Anti-Cyclin D1 antibody [SP4] (ab16663)

  Anti-Cyclin D1 antibody [SP4] (ab137875) at 1/5000 dilution + MCF-7 cell lysate
  
  Predicted band size: 33 kDa
  
  
  
  

  This image was generated from the hybridoma version.

   

• 

  Western blot - Anti-Cyclin D1 antibody [SP4] (ab16663)Image kindly supplied by Dr Karin Birkenkamp-Demtroeder through Abreview

  Lane 1 : Anti-Cyclin D1 antibody [SP4] (ab16663) at 1/200 dilution
  Lane 2 : Anti-Cyclin D1 antibody [SP4] (ab16663) at 1/400 dilution
  
  All lanes : Whole cell lysate prepared from T24 bladder cancer cells
  
  Lysates/proteins at 25 µg per lane.
  
  Secondary
  All lanes : Goat anti-rabbit IgG conjugated to HRP at 1/5000 dilution
  
  Developed using the ECL technique.
  
  Performed under reducing conditions.
  
  Predicted band size: 33 kDa
  Observed band size: 33 kDa
  
  
  Exposure time: 10 minutes
  
  
  

  Gel run under denaturing conditions 4-12% gradient.

  This image was generated from the hybridoma version.

   

  See Abreview

• 

  Western blot - Anti-Cyclin D1 antibody [SP4] (ab16663)

  Anti-Cyclin D1 antibody [SP4] (ab16663) at 1/25 dilution + MCF7 cell lysate
  
  Predicted band size: 33 kDa
  Observed band size: 36 kDawhy is the actual band size different from the predicted?
  
  
  
  

  This image was generated from the hybridoma version.

   

• 

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Cyclin D1 antibody [SP4] (ab16663)This image is courtesy of an Abreview submitted by Karin Birkenkamp-Demtroeder

  ab16663 staining Cyclin D1 in Human urinary tract tissue sections by Immunohistochemistry (IHC-P - formaldehyde-fixed, paraffin-embedded sections). Tissue was fixed with formaldehyde and blocked with 10% BSA for 30 minutes at room temperature; antigen retrieval was by heat mediation in citrate buffer. Samples were incubated with primary antibody (1/100 in PBS) for 1 hour. An undiluted HRP-conjugated Goat anti-rabbit IgG polyclonal was used as the secondary antibody.

  This image was generated from the hybridoma version.

   

  See Abreview

• 

  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Cyclin D1 antibody [SP4] (ab16663)

  Human mantle cell lymphoma stained with ab16663.

  This image was generated from the hybridoma version.

   

• 

  Anti-Cyclin D1 antibody [SP4] (ab16663)