PLOD2 Mouse Monoclonal Antibody (HRP conjugated) [Clone ID: OTI6D1]

CAT#: TA803224BM

PLOD2 mouse monoclonal antibody, clone OTI6D1 (formerly 6D1), HRP conjugated

Product Images

HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY PLOD2 (RC207610, 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-PLOD2. Positive lysates LY403652 (100ug) and LC403652 (20ug) can be purchased separately from OriGene.

• 

  Immunohistochemical staining of paraffin-embedded Adenocarcinoma of Human colon tissue using anti-PLOD2 mouse monoclonal antibody. (TA803224) Dilution: 1:150

• 

  Immunohistochemical staining of paraffin-embedded Human Kidney tissue within the normal limits using anti-PLOD2 mouse monoclonal antibody. (TA803224) Dilution: 1:150

• 

  Immunohistochemical staining of paraffin-embedded Human prostate tissue within the normal limits using anti-PLOD2 mouse monoclonal antibody. (TA803224) Dilution: 1:150

Specifications

Product Data

• Clone Name: OTI6D1
• Applications: IHC, WB
• Recommended Dilution: WB 1:2000
• Reactivities: Human, Mouse, Rat
• Host: Mouse
• Isotype: IgG1
• Clonality: Monoclonal
• Immunogen: Human recombinant protein fragment corresponding to amino acids 359-640 of human PLOD2 (NP_891988) produced in E.coli.
• 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: HRP
• Storage: Store at -20°C as received.
• Stability: Stable for 12 months from date of receipt.
• Gene Name: procollagen-lysine,2-oxoglutarate 5-dioxygenase 2
• Database Link:
  NP_891988
  Entrez Gene 5352 Human
  UniProt ID O00469
• Background: The protein encoded by this gene is a membrane-bound homodimeric enzyme that is localized to the cisternae of the rough endoplasmic reticulum. The enzyme (cofactors iron and ascorbate) catalyzes the hydroxylation of lysyl residues in collagen-like peptides. The resultant hydroxylysyl groups are attachment sites for carbohydrates in collagen and thus are critical for the stability of intermolecular crosslinks. Some patients with Ehlers-Danlos syndrome type VIB have deficiencies in lysyl hydroxylase activity. Mutations in the coding region of this gene are associated with Bruck syndrome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
• Synonyms: BRKS2; LH2; TLH

Reference Data

• Protein Pathways: Lysine degradation