Antibodies

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Western blot analysis of HIPK1 using A549 whole cell lysates
Western blot analysis SDCCAG8 using COLO205 whole cell lysates
Western blot analysis of extracts from Mouse spleen, using FAKD5 Antibody. The lane on the left was treated with blocking peptide.
Western blot analysis of MOB2 using LOVO whole cell lysates
DF8843 at 1/100 staining Rat liver tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary
Western blot analysis of MAP3K15 using COS7 whole cell lysates
Western blot analysis of LMTK1 using COLO205 whole cell lysates
Western blot analysis of PLXDC2 using LOVO whole cell lysates
Western blot analysis F111B using RAW264.7 whole cell lysates
Western blot analysis of TENS3 using K562 whole cell lysates
Western blot analysis of extracts from COS7, using CT47A Antibody. The lane on the left was treated with blocking peptide.
Western blot analysis of extracts from VERO, using KKLC1 Antibody. The lane on the left was treated with blocking peptide.

Observed bands: 20 kDa.
DF8835 at 1/100 staining Human brain cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary
DF8834 at 1/100 staining Human prostate tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary
Western blot analysis of TPD52L1 using LOVO whole cell lysates
Western blot analysis of TAL2 using HuvEc whole cell lysates
Western blot analysis of extracts from various samples, using hnRNP E1 Antibody.
 Lane 1: B16F10, treated with blocking peptide;
 Lane 2: B16F10;
 Lane 3: Rat  brain.
DF8830 at 1/100 staining Rat lung tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary
DF8829 at 1/100 staining Human breast cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22¡ãC. An HRP conjugated goat anti-rabbit antibody was used as the secondary
Western blot analysis of extracts from various samples, using CCRN4L Antibody.
 Lane 1: 3T3 treated with blocking peptide;
 Lane 2: 3T3;
 Lane 3: COS-7.
Western blot analysis of MTF1 using Jurkat whole cell lysates
Western blot analysis FHL3 using HT29 whole cell lysates
Western blot analysis of DMP1 using COS7 whole cell lysates
Western blot analysis SFRS6 using HT29 whole cell lysates

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