FRG2B Antikörper (Cy5)
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- Target Alle FRG2B Produkte
- FRG2B (FSHD Region Gene 2 Family, Member B (FRG2B))
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser FRG2B Antikörper ist konjugiert mit Cy5
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Applikation
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Kreuzreaktivität
- Human
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human FRG2B
- Isotyp
- IgG
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anti-FSHD Region Gene 2 Family, Member B (FRG2B) (AA 15-43), (N-Term) antibody
FRG2B Reaktivität: Human WB Wirt: Kaninchen Polyclonal RB28883 unconjugated
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- Applikationshinweise
- IF(IHC-P) 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
- FRG2B (FSHD Region Gene 2 Family, Member B (FRG2B))
- Andere Bezeichnung
- FRG2B (FRG2B Produkte)
- Synonyme
- FSHD region gene 2 family member B antikoerper, FRG2B antikoerper
- Hintergrund
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Synonyms: FRG2A, FRG2B, FRG2C, FRG2B_HUMAN, FSHD region gene 2 protein family member B, HSA10-FRG2, Protein FRG2-like-1.
Background: Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.
- Gen-ID
- 441581
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