ERCC1 / RAD10 (Tumor Progression Marker)(ERCC1/2683), 0.2mg/mL, Clone: [ERCC1/2683], Mouse, Monoclonal

Catalog Number: BOT-BNUB2683-500
Article Name: ERCC1 / RAD10 (Tumor Progression Marker)(ERCC1/2683), 0.2mg/mL, Clone: [ERCC1/2683], Mouse, Monoclonal
Biozol Catalog Number: BOT-BNUB2683-500
Supplier Catalog Number: BNUB2683-500
Alternative Catalog Number: BOT-BNUB2683-500-500UL
Manufacturer: Biotium
Host: Mouse
Category: Antikörper
Species Reactivity: Human
Immunogen: Recombinant fragment (around aa 191-281) of human ERCC1 protein (exact sequence is proprietary)
Alternative Names: COFS4, DNA excision repair protein ERCC1, ERCC1, Excision repair cross complementing 1, RAD10, UV20
Recognizes a protein of 110 kDa, identified as Excision Repair Cross Complementing 1 (ERCC1). It is a mammalian nucleotide excision repair (NER) enzyme involved in repair of damaged DNA. ERCC1 is a homologous to RAD10 in Saccharomyces cerevisiae, which is required in mitotic intrachromosomal recombination and repair. ERCC1 is required in repair of cisplatin-induced DNA adducts and ultraviolet (UV)-induced DNA damage. High expression of ERCC1 has been linked to tumor progression in a variety of cancers including non-small cell lung cancer (NSCLC), squamous cell carcinoma of the head, ovarian cancer and esophageal cancer. Primary antibodies are available purified, or with a selection of fluorescent CF Dyes and other labels. CF Dyes offer exceptional brightness and photostability. Note: Conjugates of blue fluorescent dyes like CF405S and CF405M are not recommended for detecting low abundance targets, because blue dyes have lower fluorescence and can give higher non-specific background than other dye colors.
Clonality: Monoclonal
Concentration: 0.2 mg/mL
Clone Designation: [ERCC1/2683]
Molecular Weight: ~110 kDa
UniProt: P07992
Buffer: PBS, 0.05% BSA, 0.05% azide
Source: Animal
Application Notes: For coating for ELISA, order Ab without BSA|Higher concentration may be required for direct detection using primary antibody conjugates than for indirect detection with secondary antibody|Optimal dilution and staining procedure for a specific application should be determined by user|Recommended starting concentrations for titration are 1-2 ug/mL for most applications, or 1 ug/million cells/100 uL for flow cytometry