COX6B1 Recombinant Rabbit Monoclonal Antibody [JE59-16]
cat.: HA722407
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human
Applications: WB, IHC-P, IF-Tissue
Clonality: Monoclonal
Clone number: JE59-16
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage buffer: 1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 10 kDa
Isotype: IgG
Immunogen: Synthetic peptide within Human COX6B1 aa 37-86 / 86.
Positive control: HepG2 cell lysate, HeLa cell lysate, Caco-2 cell lysate, human colon tissue.
Subcellular location: Mitochondrion inner membrane.
Recommended Dilutions:
  WB
  IHC-P
  IF-Tissue

1:1,000
1:8,000
1:1,000-1:4,000
Uniprot #: SwissProt: P14854 Human
Alternative names: COX 6B COX VIb 1 COX VIb-1 COX6B COX6B1 COXG COXVIb1 CX6B1_HUMAN Cytochrome c oxidase subunit 6B1 Cytochrome c oxidase subunit VIb Cytochrome c oxidase subunit VIb isoform 1 cytochrome c oxidase subunit VIb polypeptide 1 (ubiquitous) Cytochrome c oxidase subunit Vib polypeptide 1
Images
HA722407_1.jpg Fig1: Western blot analysis of COX6B1 on different lysates with Rabbit anti-COX6B1 antibody (HA722407) at 1/1,000 dilution.

Lane 1: HepG2 cell lysate
Lane 2: HeLa cell lysate
Lane 3: Caco-2 cell lysate

Lysates/proteins at 20 µg/Lane.

Predicted band size: 10 kDa
Observed band size: 10 kDa

Exposure time: 18 seconds; ECL: K1801;
4-20% 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 (HA722407) at 1/1,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.
HA722407_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human colon tissue with Rabbit anti-COX6B1 antibody (HA722407) at 1/8,000 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 (HA722407) at 1/8,000 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.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.