DDB1 Rabbit Polyclonal Antibody
cat.: R1706-21
Product Type: Rabbit polyclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IF-Cell, IHC-P, FC
Clonality: Polyclonal
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃ Avoid repeated freeze / thaw cycles.
Storage buffer: 1*PBS (pH7.4), 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 127 kDa
Isotype: IgG
Immunogen: Recombinant protein within Human DDB1 aa 151-560 / 1,140.
Positive control: Mouse colon tissue lysate, PC-12, Siha, A549, SH-SY5Y, SK-Br-3, K562, human breast, human kidney, rat brain.
Subcellular location: Nucleus. Cytoplasm.
Recommended Dilutions:
  WB
  IF-Cell
  IHC-P
  FC

1:500-1:1000
1:100-1:500
1:100-1:500
1:50-1:100
Uniprot #: SwissProt: Q16531 Human | Q3U1J4 Mouse | Q9ESW0 Rat
Alternative names: Damage specific DNA binding protein 1 Damage-specific DNA-binding protein 1 DDB 1 DDB p127 subunit Ddb1 DDB1_HUMAN DDBa DNA damage binding protein 1 DNA damage-binding protein 1 DNA damage-binding protein a HBV X-associated protein 1 UV damaged DNA binding factor UV damaged DNA binding protein 1 UV DDB 1 UV DDB1 UV-damaged DNA-binding factor UV-damaged DNA-binding protein 1 UV-DDB 1 X associated protein 1 XAP 1 XAP-1 XAP1 Xeroderma pigmentosum group E complementing protein Xeroderma pigmentosum group E-complementing protein XPCe XPE XPE BF XPE binding factor XPE-BF XPE-binding factor
Images
R1706-21_1.jpg Fig1: Western blot analysis of DDB1 on different cell lysate using anti-DDB1 antibody at 1/1,000 dilution.
Positive control:
Lane 1: Mouse colon tissue
Lane 2: PC-12
Lane 3: Siha
R1706-21_2.jpg Fig2: ICC staining DDB1 in A549 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
R1706-21_3.jpg Fig3: ICC staining DDB1 in SH-SY5Y cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
R1706-21_4.jpg Fig4: ICC staining DDB1 in SK-Br-3 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
R1706-21_5.jpg Fig5: Immunohistochemical analysis of paraffin-embedded rat brain tissue using anti-DDB1 antibody. Counter stained with hematoxylin.
R1706-21_6.jpg Fig6: Immunohistochemical analysis of paraffin-embedded human breast tissue using anti-DDB1 antibody. Counter stained with hematoxylin.
R1706-21_7.jpg Fig7: Immunohistochemical analysis of paraffin-embedded human kidney tissue using anti-DDB1 antibody. Counter stained with hematoxylin.
R1706-21_8.png Fig8: Immunohistochemical analysis of paraffin-embedded rat kidney tissue with Rabbit anti-DDB1 antibody (R1706-21) at 1/400 dilution.

The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (R1706-21) at 1/400 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
R1706-21_9.jpg Fig9: Flow cytometric analysis of K562 cells with DDB1 antibody at 1/100 dilution (red) compared with an unlabelled control (cells without incubation with primary antibody; black).
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.