FAM160B1 Antikörper (AA 521-630) (AbBy Fluor® 350)
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- Target Alle FAM160B1 Antikörper anzeigen
- FAM160B1 (Family with Sequence Similarity 160, Member B1 (FAM160B1))
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Bindungsspezifität
- AA 521-630
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser FAM160B1 Antikörper ist konjugiert mit AbBy Fluor® 350
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Applikation
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Homologie
- Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Chicken,Rabbit
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human FAM160B1
- Isotyp
- IgG
- Top Product
- Discover our top product FAM160B1 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
- FAM160B1 (Family with Sequence Similarity 160, Member B1 (FAM160B1))
- Andere Bezeichnung
- FAM160B1 (FAM160B1 Produkte)
- Synonyme
- zgc:162264 antikoerper, kiaa1600 antikoerper, KIAA1600 antikoerper, bA106M7.3 antikoerper, AI450540 antikoerper, mKIAA1600 antikoerper, RGD1306116 antikoerper, family with sequence similarity 160, member B1 antikoerper, family with sequence similarity 160 member B1 antikoerper, family with sequence similarity 160 member B1 S homeolog antikoerper, fam160b1 antikoerper, FAM160B1 antikoerper, Fam160b1 antikoerper, fam160b1.S antikoerper
- Hintergrund
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Synonyms: DKFZp686D10123, F16B1_HUMAN, Fam160b1, Family with sequence similarity 160 member B1, Hypothetical protein LOC57700, KIAA1600, Protein FAM160B1.
Background: FAM168A is a 244 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11, which makes up around 4 % of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
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