AFG3L2 anticorps (Middle Region)
Aperçu rapide pour AFG3L2 anticorps (Middle Region) (ABIN2782736)
Antigène
Voir toutes AFG3L2 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- Middle Region
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Séquence
- VNFLKNPKQY QDLGAKIPKG AILTGPPGTG KTLLAKATAG EANVPFITVS
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Homologie
- Cow: 100%, Dog: 100%, Goat: 79%, Guinea Pig: 100%, Horse: 100%, Human: 100%, Mouse: 100%, Rabbit: 100%, Rat: 100%, Yeast: 85%, Zebrafish: 100%
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Attributs du produit
- This is a rabbit polyclonal antibody against AFG3L2. 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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Immunogène
- The immunogen is a synthetic peptide directed towards the middle region of human AFG3L2
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Indications d'application
- Optimal working dilutions should be determined experimentally by the investigator.
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Commentaires
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Antigen size: 797 AA
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- Lot specific
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Buffer
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Conseil sur la manipulation
- Avoid repeated freeze-thaw cycles.
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Stock
- -20 °C
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Stockage commentaire
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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- AFG3L2 (AFG3-Like Protein 2 (AFG3L2))
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Autre désignation
- AFG3L2
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Sujet
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AFG3L2 is a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. AFG3L2 gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders.This gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders.
Alias Symbols: FLJ25993, SCA28
Protein Interaction Partner: SUMO2, UBC, SUZ12, RNF2, HIPK4, FBXO6, BTK, APP, MAPK8IP2, RAC2, ICT1, BECN1, CLN3, USP50, PHC2,
Protein Size: 797 -
Poids moléculaire
- 88 kDa
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ID gène
- 10939
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NCBI Accession
- NM_006796, NP_006787
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UniProt
- Q9Y4W6
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Pathways
- Skeletal Muscle Fiber Development
Antigène
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