TEX33 Antikörper (AA 201-280)

Produktnummer ABIN6989177

Der Kaninchen Polyklonal anti-TEX33 Antikörper wird verwendet zum Nachweis von TEX33 in Proben von Human. Er wurde validiert für IF (cc), IF (p), IHC (fro) und IHC (p).

Kurzübersicht für TEX33 Antikörper (AA 201-280) (ABIN6989177)

Target: TEX33 (Testis Expressed 33 (TEX33))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser TEX33 Antikörper ist unkonjugiert

Applikation: Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Produktdetails anti-TEX33 Antikörper

Bindungsspezifität: AA 201-280

Verwendungszweck: EAN57 Polyclonal Antibody

Kreuzreaktivität: Maus

Homologie: Human,Rat,Dog,Cow,Pig,Horse

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human EAN57

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Optimal working dilution should be determined by the investigator.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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: 4 °C,-20 °C

Informationen zur Lagerung: Shipped at 4C. Store at -20C for one year. Avoid repeated freeze/thaw cycles.

Haltbarkeit: 12 months

Details zu TEX33

Target: TEX33 (Testis Expressed 33 (TEX33))

Andere Bezeichnung: EAN57

Hintergrund:

Synonyms: C22orf33, cE81G9.2, Chromosome 22 open reading frame 33, Ean57, TEX33_HUMAN, Protein EAN57, Testis expressed sequence 33 protein, TEX33.

Background: EAN57 is a 59 amino acid protein encoded by the C22orf33 protein. Chromosome 22 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.

Gen-ID: 339669

UniProt: O43247