TMEM176A Antikörper
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- Target Alle TMEM176A Produkte
- TMEM176A (Transmembrane Protein 176A (TMEM176A))
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Reaktivität
- Ratte
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser TMEM176A Antikörper ist unkonjugiert
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Applikation
- Immunofluorescence (IF), Immunohistochemistry (IHC)
- Kreuzreaktivität
- Ratte
- Aufreinigung
- Affinity purification
- Immunogen
- KLH conjugated Synthetic peptide corresponding to Mouse TMEM176A
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- Applikationshinweise
- IHC/IF (R) 1:500-1:1000
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Buffer
- PBS, pH 7.4, 0.02 % sodium azide
- 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
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- Target
- TMEM176A (Transmembrane Protein 176A (TMEM176A))
- Andere Bezeichnung
- TMEM176A (TMEM176A Produkte)
- Synonyme
- GS188 antikoerper, HCA112 antikoerper, 0610011I04Rik antikoerper, AU040201 antikoerper, AU041743 antikoerper, Keg2 antikoerper, 0610011i04rik antikoerper, RGD1310725 antikoerper, CL1 antikoerper, transmembrane protein 176A antikoerper, TMEM176A antikoerper, Tmem176a antikoerper
- Hintergrund
- TMEM176A is a 235 amino acid multi-pass membrane protein belonging to the TMEM176 family. The gene encoding GS188 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5 % of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance.
- Gen-ID
- 66058
- UniProt
- Q9DCS1
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