DNAAF11 Mouse Monoclonal Antibody (Biotin conjugated) [Clone ID: OTI2F8]

CAT#: TA805964AM

LRRC6 mouse monoclonal antibody, clone OTI2F8 (formerly 2F8), Biotinylated

Product Images

HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY LRRC6 (RC208256, Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-LRRC6. Positive lysates LY415734 (100ug) and LC415734 (20ug) can be purchased separately from OriGene.

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  Immunohistochemical staining of paraffin-embedded Human Kidney tissue within the normal limits using anti-LRRC6 mouse monoclonal antibody. (TA805964) Dilution: 1:150

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  Immunohistochemical staining of paraffin-embedded Human liver tissue within the normal limits using anti-LRRC6 mouse monoclonal antibody. (TA805964) Dilution: 1:150

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  Immunohistochemical staining of paraffin-embedded Carcinoma of Human liver tissue using anti-LRRC6 mouse monoclonal antibody. (TA805964) Dilution: 1:150

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  Immunohistochemical staining of paraffin-embedded Adenocarcinoma of Human ovary tissue using anti-LRRC6 mouse monoclonal antibody. (TA805964) Dilution: 1:150

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Specifications

Product Data

• Clone Name: OTI2F8
• Applications: IHC, WB
• Recommended Dilution: WB 1:2000
• Reactivities: Human
• Host: Mouse
• Isotype: IgG1
• Clonality: Monoclonal
• Immunogen: Full length human recombinant protein of human LRRC6 (NP_036604) produced in HEK293T cell.
• Formulation: PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
• Concentration: 0.5 mg/ml
• Purification: Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)
• Conjugation: Biotin
• Storage: Store at -20°C as received.
• Stability: Stable for 12 months from date of receipt.
• Predicted Protein Size: 54.1 kDa
• Gene Name: leucine rich repeat containing 6
• Database Link:
  NP_036604
  Entrez Gene 23639 Human
  UniProt ID Q86X45
• Background: The protein encoded by this gene contains several leucine-rich repeat domains and appears to be involved in the motility of cilia. Defects in this gene are a cause of primary ciliary dyskinesia-19 (CILD19). Two transcript variants, one protein-coding and the other not, have been found for this gene. [provided by RefSeq, Dec 2012]
• Synonyms: CILD19; LRTP; TSLRP