ODF3B Antikörper (AbBy Fluor® 594)
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- Target Alle ODF3B Produkte
- ODF3B (Outer Dense Fiber of Sperm Tails 3B (ODF3B))
- Reaktivität
- Human, Maus, Ratte
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser ODF3B Antikörper ist konjugiert mit AbBy Fluor® 594
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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 ODF3B
- Isotyp
- IgG
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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
- ODF3B (Outer Dense Fiber of Sperm Tails 3B (ODF3B))
- Andere Bezeichnung
- ODF3B (ODF3B Produkte)
- Synonyme
- ODF3L3 antikoerper, 2010001J22Rik antikoerper, RGD1564322 antikoerper, fj19d04 antikoerper, odf3l antikoerper, si:dkeyp-1h4.4 antikoerper, wu:fj19d04 antikoerper, zgc:63985 antikoerper, outer dense fiber of sperm tails 3B antikoerper, ODF3B antikoerper, Odf3b antikoerper, odf3b antikoerper
- Hintergrund
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Synonyms: ODF3B, ODF3B_HUMAN, Odf3l3, Outer dense fiber of sperm tails 3B, Outer dense fiber protein 3-like protein 3, Outer dense fiber protein 3B.
Background: ODF3B, also known as ODF3L3 (outer dense fiber protein 3-like protein 3), is a 253 amino acid protein belonging to the ODF3 family. Existing as two isoforms produced by alternative splicing, ODF3B contains one DUF1309 repeat. The gene that encodes ODF3B maps to human chromosome 22, which contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.
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