PEX10 antibody (C-Term)
Quick Overview for PEX10 antibody (C-Term) (ABIN2775670)
Target
See all PEX10 AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- C-Term
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Purpose
- PEX10 Antibody - C-terminal region
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Sequence
- ERRHPTATPC GHLFCWECIT AWCSSKAECP LCREKFPPQK LIYLRHYR
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Predicted Reactivity
- Dog: 93%, Guinea Pig: 93%, Horse: 93%, Human: 100%, Mouse: 93%, Rat: 93%
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Characteristics
- This is a rabbit polyclonal antibody against PEX10. 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 C terminal region of human PEX10
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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 AAP42997-100UG
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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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- PEX10 (Peroxisomal Biogenesis Factor 10 (PEX10))
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Alternative Name
- PEX10
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Background
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Background Information: PEX10 is a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in PEX10 gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome.This gene encodes a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in this gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome. Alternative splicing results in two transcript variants encoding different isoforms.
Gene Name: Peroxisomal biogenesis factor 10
Alternative Symbols: NALD, PBD6A, PBD6B, RNF69
Protein Name: Peroxisome biogenesis factor 10
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Molecular Weight
- 37kDa
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Gene ID
- 5192
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NCBI Accession
- NP_002608
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UniProt
- O60683
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Pathways
- Monocarboxylic Acid Catabolic Process
Target
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