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          • Primary Antibodies ›
          • ERCC8 Antibodies

          Invitrogen

          ERCC8 Monoclonal Antibody (OTI5C9)

          View all (22) ERCC8 antibodies

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          Cite ERCC8 Monoclonal Antibody (OTI5C9)

          Additional Information:
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          • Antibody Testing Data (2)
          ERCC8 Antibody in Immunohistochemistry (Paraffin) (IHC (P))
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          ERCC8 Antibody in Immunohistochemistry (Paraffin) (IHC (P))
          Group 53 Created with Sketch.

          FIGURE: 1 / 2

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          ERCC8 Antibody (MA5-27019) in IHC (P)

          Immunohistochemistry was performed on paraffin-embedded human embryonic brain cortex tissue. To expose target proteins, heat-induced epitope retrieval by 1mM EDTA in 10mM Tris buffer (pH8.5) at 120°C for 3 min. Following antigen retrieval, tissues were probed with a ERCC8 monoclonal antibody (Product # MA5-27019) at a dilution of 1:150. {{ $ctrl.currentElement.advancedVerification.fullName }} validation info. View more
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          ERCC8 Antibody in Immunohistochemistry (Paraffin) (IHC (P))
          ERCC8 Antibody in Western Blot (WB)
          ERCC8 Monoclonal Antibody (OTI5C9)

          Product Details

          MA5-27019

          Applications
          Tested Dilution
          Publications

          Western Blot (WB)

          1:500
          -

          Immunohistochemistry (Paraffin) (IHC (P))

          1:150
          -
          Product Specifications

          Species Reactivity

          Human

          Host/Isotype

          Mouse / IgG1

          Class

          Monoclonal

          Type

          Antibody

          Clone

          OTI5C9

          Immunogen

          Full length human recombinant protein of ERCC8 produced in E.coli
          View immunogen

          Conjugate

          Unconjugated Unconjugated Unconjugated

          Form

          Liquid

          Concentration

          1 mg/mL

          Amount

          100 µg

          Purification

          Affinity Chromatography

          Storage buffer

          PBS, pH 7.3, with 1% BSA, 50% glycerol

          Contains

          0.02% sodium azide

          Storage conditions

          -20°C, Avoid Freeze/Thaw Cycles

          Shipping conditions

          Ambient (domestic); Wet ice (international)

          RRID

          AB_2723137

          Target Information

          This gene encodes a WD repeat protein, which interacts with Cockayne syndrome type B (CSB) protein and with p44 protein, a subunit of the RNA polymerase II transcription factor IIH. Mutations in this gene have been identified in patients with hereditary disease Cockayne syndrome (CS). CS cells are abnormally sensitive to ultraviolet radiation and are defective in the repair of transcriptionally active genes.

          For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

          References (0)

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          Cite this product

          Bioinformatics

          Protein Aliases: CKN1; Cockayne syndrome WD repeat protein CSA; Cockayne syndrome WD-repeat protein CSA; DNA excision repair protein ERCC-8; excision repair cross-complementation group 8; excision repair cross-complementing rodent repair deficiency, complementation group 8; unnamed protein product

          View more View less

          Gene Aliases: CKN1; CSA; ERCC8; UVSS2

          View more View less

          UniProt ID: (Human) Q13216

          View more View less

          Entrez Gene ID: (Human) 1161

          View more View less

          Function(s)
          protein binding protein binding, bridging involved in substrate recognition for ubiquitination
          Process(es)
          single strand break repair protein polyubiquitination DNA repair transcription-coupled nucleotide-excision repair cellular response to DNA damage stimulus response to oxidative stress response to UV response to X-ray response to auditory stimulus protein ubiquitination proteasome-mediated ubiquitin-dependent protein catabolic process positive regulation of DNA repair protein autoubiquitination regulation of transcription-coupled nucleotide-excision repair double-strand break repair via classical nonhomologous end joining
          It has to be done as per old AB suggested Products section.

          Disclaimer

          Close

          Clicking the images or links will redirect you to a website hosted by BenchSci that provides third-party scientific content. Neither the content nor the BenchSci technology and processes for selection have been evaluated by us; we are providing them as-is and without warranty of any kind, including for use or application of the Thermo Fisher Scientific products presented.

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          If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*

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