FAM101A Antikörper (AA 111-216) (AbBy Fluor® 647)
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- Target Alle FAM101A Produkte
- FAM101A (Family with Sequence Similarity 101, Member A (FAM101A))
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Bindungsspezifität
- AA 111-216
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser FAM101A Antikörper ist konjugiert mit AbBy Fluor® 647
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Applikation
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Homologie
- Human,Mouse,Rat,Cow,Sheep,Pig,Horse
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human FAM101A
- 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
- FAM101A (Family with Sequence Similarity 101, Member A (FAM101A))
- Andere Bezeichnung
- FAM101A (FAM101A Produkte)
- Synonyme
- cfm antikoerper, si:bz71m17.1 antikoerper, si:rp71-71m17.1 antikoerper, 3110032G18Rik antikoerper, cfm2 antikoerper, refilin A antikoerper, family with sequence similarity 101, member A antikoerper, rflna antikoerper, RFLNA antikoerper, Rflna antikoerper, FAM101A antikoerper
- Hintergrund
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Synonyms: cfm, 3110032G18Rik, cfm2, F101A_HUMAN, FAM101A, Family with sequence similarity 101, member A, FLJ44614, Hypothetical protein LOC73121, Protein FAM101A.
Background: Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5 % of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The FAM101A gene product has been provisionally designated FAM101A pending further characterization.
- Gen-ID
- 144347
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