ABHD5 anticorps
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- Antigène Voir toutes ABHD5 Anticorps
- ABHD5 (Abhydrolase Domain Containing 5 (ABHD5))
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Monoclonal
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Conjugué
- Cet anticorp ABHD5 est non-conjugé
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Application
- Western Blotting (WB)
- Fonction
- ABHD5 Rabbit mAb
- Réactivité croisée
- Humain, Rat
- Attributs du produit
- Monoclonal Antibodies
- Purification
- Affinity purification
- Immunogène
- A synthesized peptide derived from human ABHD5
- Isotype
- IgG
- Top Product
- Discover our top product ABHD5 Anticorps primaire
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- Indications d'application
- WB,1:500 - 1:2000
- Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20°C. Avoid freeze / thaw cycles.
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- Antigène
- ABHD5 (Abhydrolase Domain Containing 5 (ABHD5))
- Autre désignation
- ABHD5 (ABHD5 Produits)
- Synonymes
- anticorps ABHD5, anticorps cds, anticorps cgi58, anticorps iecn2, anticorps ncie2, anticorps abhd5, anticorps CDS, anticorps CGI58, anticorps IECN2, anticorps NCIE2, anticorps 1300003D03Rik, anticorps 2010002J10Rik, anticorps CGI-58, anticorps IECN5, anticorps abhydrolase domain containing 5, anticorps abhydrolase domain containing 5a, anticorps abhydrolase domain containing 5 L homeolog, anticorps ABHD5, anticorps abhd5, anticorps abhd5a, anticorps Abhd5, anticorps abhd5.L
- Sujet
- The protein encoded by this gene belongs to a large family of proteins defined by an alpha/beta hydrolase fold, and contains three sequence motifs that correspond to a catalytic triad found in the esterase/lipase/thioesterase subfamily. It differs from other members of this subfamily in that its putative catalytic triad contains an asparagine instead of the serine residue. Mutations in this gene have been associated with Chanarin-Dorfman syndrome, a triglyceride storage disease with impaired long-chain fatty acid oxidation. [provided by RefSeq, Jul 2008],CDS, CGI58, IECN2, NCIE2,Cancer,Cardiovascular,Endocrine & Metabolism,Endocrine and metabolic diseases,Endocrine and metabolic diseases_Obesity,Lipid Metabolism,Lipids,Lipids_Adipose Related,Lipids_Fatty Acids,Signal Transduction,ABHD5
- Poids moléculaire
- 45kDa
- ID gène
- 51099
- UniProt
- Q8WTS1
- Pathways
- Lipid Metabolism
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