DAZL Recombinant Rabbit Monoclonal Antibody [JA10-36]
cat.: ET1704-75
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IHC-P
Clonality: Monoclonal
Clone number: JA10-36
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles.
Storage buffer: 1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1 mg/mL.
Purification: Protein A affinity purified.
Molecular weight: 33 kDa
Isotype: IgG
Immunogen: Synthetic peptide within DAZL aa 10-59 / 295.
Positive control: Rat testis tissue, mouse testis tissue.
Subcellular location: Cytoplasm. Nucleus. Predominantly cytoplasmic.
Recommended Dilutions:
  WB
  IHC-P

1:500
1:50
Uniprot #: SwissProt: Q92904 Human | Q64368 Mouse
Alternative names: DAZ homolog DAZ like autosomal DAZ-like autosomal DAZH DAZL 1 DAZL DAZL_HUMAN DAZL1 DAZLA Deleted in azoospermia like 1 Deleted in azoospermia like Deleted in azoospermia like autosomal Deleted in azoospermia-like 1 Deleted in azoospermia-like Germline specific RNA binding protein MGC26406 Spermatogenesis gene on the Y like autosomal SPGY like autosomal SPGY-like-autosomal SPGYLA Tpx2
Images
ET1704-75_1.jpg Fig1: Immunohistochemical analysis of paraffin-embedded rat testis tissue using anti-DAZL antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes.The tissues were blocked in 1% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1704-75, 1/50) for 30 minutes 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.
ET1704-75_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded mouse testis tissue using anti-DAZL antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes.The tissues were blocked in 1% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1704-75, 1/50) for 30 minutes 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.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.