TEX33 anticorps (AA 201-280) (AbBy Fluor® 488)
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- Antigène Tous les produits TEX33
- TEX33 (Testis Expressed 33 (TEX33))
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Épitope
- AA 201-280
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Reactivité
- Souris
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp TEX33 est conjugé à/à la AbBy Fluor® 488
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Application
- Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunofluorescence (Cultured Cells) (IF (cc))
- Réactivité croisée
- Souris
- Homologie
- Human,Rat,Dog,Cow,Pig,Horse
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human EAN57
- Isotype
- IgG
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- Indications d'application
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- Agent conservateur
- ProClin
- Précaution d'utilisation
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Date de péremption
- 12 months
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- Antigène
- TEX33 (Testis Expressed 33 (TEX33))
- Autre désignation
- EAN57 (TEX33 Produits)
- Synonymes
- anticorps C22orf33, anticorps EAN57, anticorps cE81G9.2, anticorps 1700061J05Rik, anticorps Ean57, anticorps testis expressed 33, anticorps TEX33, anticorps Tex33
- Sujet
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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.
- ID gène
- 339669
- UniProt
- O43247
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