Product Type: | Rabbit polyclonal IgG, primary antibodies |
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Species reactivity: | Human, Rat |
Applications: | WB, IHC-P, IF-Cell |
Clonality: | Polyclonal |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles. |
Storage buffer: | PBS (pH7.4), 0.1% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide. |
Concentration: | 1ug/ul |
Purification: | Immunogen affinity purified. |
Molecular weight: | Predicted band size: 25 kDa |
Isotype: | IgG |
Immunogen: | Recombinant protein within human CLTB aa 30-229 / 229. |
Positive control: | MCF-7 cell lysate, Hela cell lysate, 293T cell lysate, human placenta tissue lysate, rat testis tissue, SiHa. |
Subcellular location: | Cytoplasmic vesicle membrane, Membrane, coated pit. |
Recommended Dilutions:
WB IHC-P IF-Cell |
1:500 1:600 1:100 |
Uniprot #: | SwissProt: P09497 Human | P08082 Rat |
Alternative names: | Clathrin light chain B Clathrin light chain LCB Clathrin light polypeptide B Clathrin light polypeptide LCB Clathrin, light chain (Lcb) Clathrin, light polypeptide (Lcb) CLTB LCB |
Fig1:
Western blot analysis of CLTB on different lysates with Rabbit anti-CLTB antibody (HA500451) at 1/500 dilution. Lane 1: MCF-7 cell lysate (10 µg/Lane) Lane 2: Hela cell lysate (20 µg/Lane) Lane 3: 293T cell lysate (10 µg/Lane) Lane 4: Human placenta tissue lysate (20 µg/Lane) Predicted band size: 25 kDa Observed band size: 25 kDa Exposure time: 2 minutes; 15% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA500451) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:300,000 dilution was used for 1 hour at room temperature. |
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Fig2:
Immunohistochemical analysis of paraffin-embedded rat testis tissue with Rabbit anti-CLTB antibody (HA500451) at 1/600 dilution. 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 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA500451) at 1/600 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. |
Fig3:
Immunocytochemistry analysis of SiHa cells labeling CLTB with Rabbit anti-CLTB antibody (HA500451) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.05% Triton X-100 in PBS for 20 minutes, and then blocked with 2% negative goat serum for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-CLTB antibody (HA500451) at 1/100 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. Nuclear DNA was labelled in blue with DAPI. Beta tubulin (M1305-2, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 647, HA1127) was used as the secondary antibody at 1/1,000 dilution. |