ERCC8 antibody (N-Term)
Quick Overview for ERCC8 antibody (N-Term) (ABIN2779478)
Target
See all ERCC8 AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- N-Term
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Purpose
- ERCC8 Antibody - N-terminal region
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Sequence
- DVERIHGGGI NTLDIEPVEG RYMLSGGSDG VIVLYDLENS SRQSYYTCKA
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Predicted Reactivity
- Cow: 77%, Dog: 85%, Guinea Pig: 77%, Human: 100%, Mouse: 85%, Pig: 85%, Rabbit: 85%, Rat: 77%, Zebrafish: 85%
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Characteristics
- This is a rabbit polyclonal antibody against ERCC8. It was validated on Western Blot using a cell lysate as a positive control.
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Purification
- Affinity Purified
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Immunogen
- The immunogen is a synthetic peptide directed towards the N terminal region of human ERCC8
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Application Notes
- Optimal working dilution should be determined by the investigator.
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Comment
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We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP32149-100UG
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 0.5 mg/mL
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Buffer
- Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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Preservative
- Sodium azide
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Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Handling Advice
- prevent freeze-thaw cycles
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Storage
- 4 °C,-20 °C
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Storage Comment
- For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.
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- ERCC8 (Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 8 (ERCC8))
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Alternative Name
- ERCC8
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Background
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Background Information: ERCC8 is 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). 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.
Gene Name: Excision repair cross-complementing rodent repair deficiency, complementation group 8
Alternative Symbols: CSA, CKN1, UVSS2
Protein Name: DNA excision repair protein ERCC-8
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Molecular Weight
- 44kDa
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Gene ID
- 1161
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NCBI Accession
- NP_000073
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UniProt
- Q13216
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Pathways
- DNA Damage Repair, Positive Regulation of Response to DNA Damage Stimulus
Target
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