FAM81A Antikörper (AA 281-368) (AbBy Fluor® 750)
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- Target Alle FAM81A Produkte
- FAM81A (Family with Sequence Similarity 81, Member A (FAM81A))
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Bindungsspezifität
- AA 281-368
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser FAM81A Antikörper ist konjugiert mit AbBy Fluor® 750
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Applikation
- Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunofluorescence (Cultured Cells) (IF (cc))
- Homologie
- Human,Mouse,Rat
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human FAM81A
- Isotyp
- IgG
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- Applikationshinweise
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- Konservierungsmittel
- ProClin
- Vorsichtsmaßnahmen
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Haltbarkeit
- 12 months
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- Target
- FAM81A (Family with Sequence Similarity 81, Member A (FAM81A))
- Andere Bezeichnung
- FAM81A (FAM81A Produkte)
- Synonyme
- 6430514L14Rik antikoerper, RGD1311958 antikoerper, family with sequence similarity 81, member A antikoerper, family with sequence similarity 81 member A antikoerper, Fam81a antikoerper, FAM81A antikoerper
- Hintergrund
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Synonyms: FA81B_HUMAN, FAM81B, Family with sequence similarity 81, member B, FLJ25333, Hypothetical protein LOC153643, Protein FAM81B.
Background: Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3 % of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The FAM81A gene product has been provisionally designated FAM81A pending further characterization.
- Gen-ID
- 145773
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