CXorf56 Antikörper (AA 120-170) (AbBy Fluor® 680)
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- Target Alle CXorf56 (CXORF56) Antikörper anzeigen
- CXorf56 (CXORF56) (Chromosome X Open Reading Frame 56 (CXORF56))
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Bindungsspezifität
- AA 120-170
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Reaktivität
- Human, Maus, Ratte
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser CXorf56 Antikörper ist konjugiert mit AbBy Fluor® 680
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Applikation
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Kreuzreaktivität
- Human, Maus, Ratte
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human CXorf56
- Isotyp
- IgG
- Top Product
- Discover our top product CXORF56 Primärantikörper
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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
- CXorf56 (CXORF56) (Chromosome X Open Reading Frame 56 (CXORF56))
- Andere Bezeichnung
- CXorf56 (CXORF56 Produkte)
- Synonyme
- C4HXorf56 antikoerper, CXorf56 antikoerper, c330007p06-a antikoerper, cxorf56 antikoerper, chromosome X open reading frame 56 antikoerper, chromosome 4 CXorf56 homolog antikoerper, chromosome X open reading frame, human CXorf56 antikoerper, RIKEN cDNA C330007P06 gene antikoerper, chromosome X open reading frame 56 L homeolog antikoerper, CXorf56 antikoerper, C4HXorf56 antikoerper, CXHXorf56 antikoerper, C330007P06Rik antikoerper, cxorf56.L antikoerper
- Hintergrund
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Synonyms: UPF0428 protein CXorf56, CXorf56
Background: The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unsual number and combination of sex chromosomes being inherited. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome. The CXorf56 gene product has been provisionally designated CXorf56 pending further characterization.
- Gen-ID
- 63932
- UniProt
- Q9H5V9
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