PAFAH1B3 anticorps
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- Antigène Voir toutes PAFAH1B3 Anticorps
- PAFAH1B3 (Platelet-Activating Factor Acetylhydrolase 1b, Catalytic Subunit 3 (29kDa) (PAFAH1B3))
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp PAFAH1B3 est non-conjugé
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Application
- Western Blotting (WB)
- Purification
- Affinity purification
- Immunogène
- Recombinant Protein of human PAFAH1B3
- Isotype
- IgG
- Top Product
- Discover our top product PAFAH1B3 Anticorps primaire
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- Indications d'application
- WB 1:500 - 1:2000
- Commentaires
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In the adult, expressed in brain, skeletal muscle, kidney, thymus, spleen, colon, testis, ovary and peripheral blood leukocytes, In the fetus, highest expression occurs in brain
- Restrictions
- For Research Use only
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- Buffer
- PBS with 0.02 % sodium azide, 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 -20C. Avoid freeze / thaw cycles.
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- Antigène
- PAFAH1B3 (Platelet-Activating Factor Acetylhydrolase 1b, Catalytic Subunit 3 (29kDa) (PAFAH1B3))
- Autre désignation
- PAFAH1B3 (PAFAH1B3 Produits)
- Synonymes
- anticorps PAFAHG, anticorps Pafahg, anticorps mus[g], anticorps platelet activating factor acetylhydrolase 1b catalytic subunit 3, anticorps platelet-activating factor acetylhydrolase 1b, catalytic subunit 3, anticorps platelet-activating factor acetylhydrolase, isoform 1b, subunit 3, anticorps PAFAH1B3, anticorps Pafah1b3
- Sujet
- This gene encodes an acetylhydrolase that catalyzes the removal of an acetyl group from the glycerol backbone of platelet-activating factor. The encoded enzyme is a subunit of the platelet-activating factor acetylhydrolase isoform 1B complex, which consists of the catalytic beta and gamma subunits and the regulatory alpha subunit. This complex functions in brain development. A translocation between this gene on chromosome 19 and the CDC-like kinase 2 gene on chromosome 1 has been observed, and was associated with mental retardation, ataxia, and atrophy of the brain. Alternatively spliced transcript variants have been described.
- Poids moléculaire
- 25.734 kDa
- ID gène
- 5050
- UniProt
- Q15102
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