FA2H Antikörper
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- Target Alle FA2H Antikörper anzeigen
- FA2H (Fatty Acid 2-Hydroxylase (FA2H))
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Reaktivität
- Human, Ratte
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser FA2H Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), Immunohistochemistry (IHC)
- Produktmerkmale
- Polyclonal Antibody
- Aufreinigung
- Affinity purification
- Immunogen
- Recombinant fusion protein of human FA2H (NP_077282.3).
- Isotyp
- IgG
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- Applikationshinweise
- WB 1:500-1:2000 IHC 1:50-1:200
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1 mg/mL
- Buffer
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- FA2H (Fatty Acid 2-Hydroxylase (FA2H))
- Andere Bezeichnung
- FA2H (FA2H Produkte)
- Synonyme
- FAAH antikoerper, FAH1 antikoerper, FAXDC1 antikoerper, SCS7 antikoerper, SPG35 antikoerper, RGD1310347 antikoerper, Wdr59 antikoerper, Faxdc1 antikoerper, G630055L08Rik antikoerper, MGC85470 antikoerper, MGC97767 antikoerper, cb1044 antikoerper, zgc:153777 antikoerper, fatty acid 2-hydroxylase antikoerper, fatty acid 2-hydroxylase L homeolog antikoerper, fatty acid hydroxylase antikoerper, FA2H antikoerper, Fa2h antikoerper, fa2h.L antikoerper, fa2h antikoerper, Tsp_11648 antikoerper, Ilyop_0703 antikoerper, Celly_1453 antikoerper, Weevi_1515 antikoerper, Fluta_1455 antikoerper, Mesop_3301 antikoerper
- Hintergrund
- This gene encodes a protein that catalyzes the synthesis of 2-hydroxysphingolipids, a subset of sphingolipids that contain 2-hydroxy fatty acids. Sphingolipids play roles in many cellular processes and their structural diversity arises from modification of the hydrophobic ceramide moiety, such as by 2-hydroxylation of the N-acyl chain, and the existence of many different head groups. Mutations in this gene have been associated with leukodystrophy dysmyelinating with spastic paraparesis with or without dystonia.
- Molekulargewicht
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Observed_MW: 38 kDa
Calculated_MW: 18 kDa/42 kDa
- Gen-ID
- 79152
- UniProt
- Q7L5A8
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