Bio-Connect

Antibodies

We offer one of the most comprehensive portfolios of antibodies. This includes monoclonal and polyclonal primary, secondary, conjugated, phospho-specific, functional, (isotype) controls, tagged and antibody pairs. In addition, we offer custom antibody services from several manufacturers.

The antibodies are generated in various hosts and react to antigens of different species like human, mouse, rat, rabbit or zebrafish. The antibodies are validated for multiple applications, including immunohistochemistry, western blot, immunoprecipitation, ELISA and flow cytometry, to ensure reliable performance for your research needs.

If you need a specific antibody and can’t find it in our webshop, please contact our technical support.

Discover what our customers say about us by reading their reviews.

229 to 240 of 41.447 products
Sort by
ChIP analysis of 2 microg of J1 ES genomic DNA spiked with 1 pg of a control DNA fragment (approximately 700 bp from the RFP (Ring finger protein) gene) containing different cytosine modifications using GTX60801 5-Carboxylcytosine / 5-caC antibody. The mC and hmC control DNA was generated by PCR with the corresponding nucleotide. The caC control fragment was obtained by in vitro methylation using M.SssI methyltransferase followed by oxidation with purified Tet2. The IPd DNA was subsequently anaysed by qPCR using primers specific for the control DNA fragments and for GAPDH, used as a negative control.
Product group Antibodies
References
GeneTex
ApplicationsDot Blot, ImmunoFluorescence, ImmunoPrecipitation, ChIP Chromatin ImmunoPrecipitation, ImmunoCytoChemistry
ReactivityOther Species
  • SizePrice
Dot blot analysis of 100 to 4 ng (equivalent of 5 to 0.2 pmol of C-bases) of the hmC, mC and C PCR controls using GTX60802 5-Hydroxymethylcytosine / 5-hmC antibody - MeDIP grade. Dilution : 1:200
Product group Antibodies
GeneTex
ApplicationsDot Blot, ELISA, Other Application
ReactivityOther Species
  • SizePrice
Dot blot analysis of 4 - 100 ng (equivalent of 5 to 0.2 pmol of C-bases) hmC, mC and C controls using GTX60803 5-Methylcytosine / 5-mC antibody [GT9076]. Dilution : 1:600
Product group Antibodies
GeneTex
ApplicationsDot Blot, ImmunoFluorescence, ImmunoCytoChemistry, Other Application
ReactivityOther Species
  • SizePrice
WB analysis of whole cell extracts (WCE) from drosophila larva and drosophila adults (Figure 1A) or on nuclear extracts from HeLa cells (HeLa NE, 20 microg) (Figure 1B) using GTX60804 CDC73 antibody - ChIP grade. Dilution : 1:1,000
Product group Antibodies
GeneTex
ApplicationsImmunoPrecipitation, Western Blot, ChIP Chromatin ImmunoPrecipitation
ReactivityDrosophila, Human
TargetCDC73
  • SizePrice
ChIP analysis of sheared chromatin from 4x10? K562 cells using GTX60811 EZH2 antibody - ChIP grade. A titration of the antibody consisting of 1, 2. 5 and 10 microg per ChIP experiment was analysed. IgG (2 microg/IP) was used as negative IP control. Quantitative PCR was performed with primers for MYT1 and HOXA9, used as positive control targets, and for the coding regions of the active CCT5 and EIF2S3 genes, used as negative controls. This figure shows the recovery, expressed as a % of input (the relative amount of immunoprecipitated DNA compared to input DNA after qPCR analysis).
Product group Antibodies
GeneTex
ApplicationsImmunoFluorescence, Western Blot, ChIP Chromatin ImmunoPrecipitation, ImmunoCytoChemistry, Other Application
ReactivityHuman, Mouse
TargetEzh2
  • SizePrice
ChIP analysis of sheared chromatin from 10? HeLa cells using GTX60812 Histone H2A.Z antibody - ChIP grade. A titration of the antibody consisting of 0.2, 0.5, 1 and 2 microg per ChIP experiment was analysed. IgG (1 microg/IP) was used as negative IP control. Quantitative PCR was performed with primers specific for the promoter of the active genes c-fos and EIF2S3, used as positive controls, and for the coding region of the inactive MB gene and the Sat2 satellite repeat, used as negative controls. This figure shows the recovery, expressed as a % of input (the relative amount of immunoprecipitated DNA compared to input DNA after qPCR analysis).
Product group Antibodies
GeneTex
ApplicationsImmunoFluorescence, Western Blot, ChIP Chromatin ImmunoPrecipitation, ELISA, ImmunoCytoChemistry
ReactivityHuman
TargetH2AZ1
  • SizePrice
ChIP analysis of sheared chromatin from 10? HeLa cells using GTX60813 Histone H2A.Z (acetyl Lys4/Lys7/Lys11) antibody - ChIP grade. A titration of the antibody consisting of 0.2, 0.5, 1 and 2 microg per ChIP experiment was analysed. IgG (1 microg/IP) was used as negative IP control. Quantitative PCR was performed with primers specific for the promoter of the active genes CCT5 and EIF4A2, used as positive controls, and for the coding region of the inactive MYT1 gene and the Sat2 satellite repeat, used as negative controls. This figure shows the recovery, expressed as a % of input (the relative amount of immunoprecipitated DNA compared to input DNA after qPCR analysis).
Product group Antibodies
References
GeneTex
ApplicationsDot Blot, ImmunoFluorescence, Western Blot, ChIP Chromatin ImmunoPrecipitation, ELISA, ImmunoCytoChemistry
ReactivityHuman, Mouse
TargetH2AZ1
  • SizePrice
ChIP analysis of sheared chromatin from 10? HeLa cells treated with TSA using GTX60814 Histone H3K18ac (Acetyl Lys18) antibody - ChIP grade. A titration consisting of 1, 2, 5 and 10 microg of antibody per ChIP experiment was analyzed. IgG (2 microg/IP) was used as a negative IP control. Quantitative PCR was performed with primers for the promoters of the active EIF4A2 and c-fos genes, used as positive controls, and for the inactive MYOD1 gene and the Sat2 satellite repeat, used as negative controls. This figure shows the recovery, expressed as a % of input (the relative amount of immunoprecipitated DNA compared to input DNA after qPCR analysis).
Product group Antibodies
GeneTex
ApplicationsDot Blot, ImmunoFluorescence, Western Blot, ChIP Chromatin ImmunoPrecipitation, ELISA, ImmunoCytoChemistry
ReactivityHuman, Mouse
TargetH3C1
  • SizePrice
ChIP analysis of sheared chromatin from 10? HeLa cells using GTX60815 Histone H3K27ac (Acetyl Lys27) antibody - ChIP grade. A titration consisting of 0.2, 0.5, 1 and 2 microg of antibody per ChIP experiment was analyzed. IgG (1 microg/IP) was used as a negative IP control. Quantitative PCR was performed with primers for the promoters of the active GAPDH and EIF4A2 genes, used as positive controls, and for the coding regions of the inactive MB and MYT1 genes, used as negative controls. This figure shows the recovery, expressed as a % of input (the relative amount of immunoprecipitated DNA compared to input DNA after qPCR analysis).
Product group Antibodies
References
GeneTex
ApplicationsDot Blot, ImmunoFluorescence, Western Blot, ChIP Chromatin ImmunoPrecipitation, ELISA, ImmunoCytoChemistry
ReactivityHuman, Mouse, Plant, Rat
  • SizePrice
ChIP analysis of sheared chromatin from 10? HeLa cells using GTX60816 Histone H3K27me3 (Tri-methyl Lys27) antibody - ChIP grade. A titration consisting of 0.5, 1, 2 and 5 microg of antibody per ChIP experiment was analyzed. IgG (1 microg/IP) was used as a negative IP control. Figure 1A. Quantitative PCR was performed with primers specific for the promoter of the active GAPDH and EIF4A2 genes, used as negative controls, and for the inactive TSH2B and MYT1 genes, used as positive controls. The graph shows the recovery, expressed as a % of input (the relative amount of immunoprecipitated DNA compared to input DNA after qPCR analysis). Figure 1B. Recovery of the nucleosomes carrying the H3K27me1, H3K27me2, H3K27me3, H3K4me3, H3K9me3 and H3K36me3 modifications and the unmodified H3K27 as determined by qPCR. The figure clearly shows the antibody is very specific in ChIP for the H3K27me3 modification.
Product group Antibodies
GeneTex
ApplicationsDot Blot, ImmunoFluorescence, Western Blot, ChIP Chromatin ImmunoPrecipitation, ELISA, ImmunoCytoChemistry
ReactivityAlgae, C. Elegans, Drosophila, Human, Mouse, Plant, Other Species
  • SizePrice
ChIP analysis of sheared chromatin from 10? HeLa cells using GTX60817 Histone H3K36me3 (Tri-methy Lys36) antibody - ChIP grade. A titration consisting of 0.2, 0.5, 1 and 2 microg of antibody per ChIP experiment was analyzed. IgG (1 microg/IP) was used as a negative IP control. Quantitative PCR was performed with primers for the coding region of the active GAPDH and ACTB genes, used as positive controls, and for the coding region of the inactive MB gene and the Sat satellite repeat, used as negative controls. This figure shows the recovery, expressed as a % of input (the relative amount of immunoprecipitated DNA compared to input DNA after qPCR analysis).
Product group Antibodies
GeneTex
ApplicationsDot Blot, ImmunoFluorescence, Western Blot, ChIP Chromatin ImmunoPrecipitation, ELISA, ImmunoCytoChemistry, Other Application
ReactivityHuman, Mouse, Plant
TargetH3C1
  • SizePrice
ChIP analysis of sheared chromatin from 10? K562 cells using GTX60818 Histone H3K4me1 (Mono-methyl Lys4) antibody - ChIP grade. A titration consisting of 1, 2, 5 and 10 microg of antibody per ChIP experiment was analyzed. IgG (1 microg/IP) was used as a negative IP control. Quantitative PCR was performed with primers for a region surrounding the ACTB and GAS2L1 gene, respectively, used as positive controls, and for the promoters of the GAPDH and EIF4A2 genes, used as negative controls. Figure 2 shows the recovery, expressed as a % of input (the relative amount of immunoprecipitated DNA compared to input DNA after qPCR analysis).
Product group Antibodies
References
GeneTex
ApplicationsDot Blot, ImmunoFluorescence, Western Blot, ChIP Chromatin ImmunoPrecipitation, ELISA, ImmunoCytoChemistry, Other Application
ReactivityHuman, Mouse
TargetH3C1
  • SizePrice