SCRN2 Antikörper
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- Target Alle SCRN2 Antikörper anzeigen
- SCRN2 (Secernin 2 (SCRN2))
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Reaktivität
- Human, Maus, Ratte
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser SCRN2 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), Immunohistochemistry (IHC), ELISA
- Produktmerkmale
- Polyclonal Antibody
- Aufreinigung
- Antigen affinity purification
- Immunogen
- Fusion protein of human SCRN2
- Isotyp
- IgG
- Top Product
- Discover our top product SCRN2 Primärantikörper
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- Applikationshinweise
- WB 1:500-1:2000, IHC 1:50-1:300, ELISA 1:5000-1:10000
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1.08 mg/mL
- Buffer
- PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
- 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
- SCRN2 (Secernin 2 (SCRN2))
- Andere Bezeichnung
- SCRN2 (SCRN2 Produkte)
- Synonyme
- MGC147610 antikoerper, si:ch211-184m19.2 antikoerper, Ses2 antikoerper, AV001119 antikoerper, D11Moh48 antikoerper, SES2 antikoerper, secernin 2 antikoerper, secernin 2 S homeolog antikoerper, SCRN2 antikoerper, scrn2 antikoerper, scrn2.S antikoerper, Scrn2 antikoerper
- Hintergrund
- The SCRN (Secernin) gene family has three vertebrate paralogs, i.e. SCRN1, SCRN2 and SCRN3, which are closely linked to human HOXA, HOXB and HOXD cluster, respectively. SCRN2 (secernin-2) is a 425 amino acid protein that belongs to the peptidase C69 family and the Secernin subfamily. Vertebrate SCRN genes showed a topology of the form (A)(BC), i.e. (Hsa2 Hsa7)(Hsa17), with SCRN2 falling outside the SCRN3-SCRN1 cluster. The SCRN2 gene is conserved in dog, cow, mouse, rat and zebrafish, and maps to human chromosome 17q21.32. Chromosome 17 makes up over 2.5 % of the human genome with about 81 million bases encoding over 1,200 genes. Chromosome 17 is linked to neurofibromatosis, a condition characterized by neural and epidermal lesions, and dysregulated Schwann cell growth. Alexander disease, Birt-Hogg-Dube syndrome and Canavan disease are also associated with chromosome 17.
- Molekulargewicht
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Observed_MW: Refer to figures
Calculated_MW: 47 kDa
- UniProt
- Q96FV2
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