CXX1 Antikörper (AA 121-209) (AbBy Fluor® 555)
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- Target Alle CXX1 (FAM127A) Antikörper anzeigen
- CXX1 (FAM127A) (Family with Sequence Similarity 127, Member A (FAM127A))
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Bindungsspezifität
- AA 121-209
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser CXX1 Antikörper ist konjugiert mit AbBy Fluor® 555
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Applikation
- Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunofluorescence (Cultured Cells) (IF (cc))
- Kreuzreaktivität
- Human
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human Cerebral protein 5/CXX1
- Isotyp
- IgG
- Top Product
- Discover our top product FAM127A 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
- CXX1 (FAM127A) (Family with Sequence Similarity 127, Member A (FAM127A))
- Andere Bezeichnung
- CXX1 (FAM127A Produkte)
- Synonyme
- CXX1 antikoerper, MAR8C antikoerper, MART8C antikoerper, Mar8 antikoerper, Mart8 antikoerper, retrotransposon Gag like 8C antikoerper, RTL8C antikoerper
- Hintergrund
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Synonyms: Cerebral protein 5, CAAX box protein 1, CXX 1, FAM127A, Family with sequence similarity 127, member A, Mammalian retrotransposon derived protein 8C, Mar8, MAR8C, Mart8, MART8C, CXX1_HUMAN.
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 CXX1 gene product has been provisionally designated CXX1 pending further characterization.
- Gen-ID
- 8933
- UniProt
- A6ZKI3
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