TMEM166 Antikörper (AA 51-152) (AbBy Fluor® 680)
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- Target Alle TMEM166 (FAM176A) Antikörper anzeigen
- TMEM166 (FAM176A) (Family with Sequence Similarity 176, Member A (FAM176A))
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Bindungsspezifität
- AA 51-152
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser TMEM166 Antikörper ist konjugiert mit AbBy Fluor® 680
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Applikation
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Homologie
- Human,Mouse,Rat,Cow,Pig,Horse
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human TMEM166
- Isotyp
- IgG
- Top Product
- Discover our top product FAM176A Primärantikörper
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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
- TMEM166 (FAM176A) (Family with Sequence Similarity 176, Member A (FAM176A))
- Andere Bezeichnung
- TMEM166 (FAM176A Produkte)
- Synonyme
- Fam176a antikoerper, RGD1559797 antikoerper, Tmem166 antikoerper, FAM176A antikoerper, TMEM166 antikoerper, BC014699 antikoerper, eva-1 homolog A, regulator of programmed cell death antikoerper, eva-1 homolog A (C. elegans) antikoerper, Eva1a antikoerper, EVA1A antikoerper
- Hintergrund
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Synonyms: FLJ13391, TMEM 166, Transmembrane protein 166, EVA1A_HUMAN.
Background: TMEM166, also known as FAM176A (family with sequence similarity 176, member A), is a 152 amino acid protein encoded by a gene mapping to human chromosome 2. The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes.
- Gen-ID
- 84141
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