BCL7B anticorps (AbBy Fluor® 488)
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- Antigène Voir toutes BCL7B Anticorps
- BCL7B (B-Cell CLL/lymphoma 7B (BCL7B))
- Reactivité
- Humain, Souris, Rat
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp BCL7B est conjugé à/à la AbBy Fluor® 488
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Application
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Réactivité croisée
- Humain, Souris, Rat
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human BCL7B
- Isotype
- IgG
- Top Product
- Discover our top product BCL7B Anticorps primaire
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- Indications d'application
- IF(IHC-P) 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
- BCL7B (B-Cell CLL/lymphoma 7B (BCL7B))
- Autre désignation
- BCL7B (BCL7B Produits)
- Synonymes
- anticorps bcl7b, anticorps zgc:103501, anticorps wu:fb94h01, anticorps zgc:85678, anticorps B-cell CLL/lymphoma 7B, b, anticorps B-cell CLL/lymphoma 7B, a, anticorps B-cell CLL/lymphoma 7B, anticorps B-cell CLL/lymphoma 7b, anticorps B cell CLL/lymphoma 7B, anticorps BCL tumor suppressor 7B, anticorps bcl7bb, anticorps bcl7ba, anticorps bcl7b, anticorps Bcl7b, anticorps BCL7B
- Sujet
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Synonyms: B cell CLL/lymphoma 7 protein family member B, B cell CLL/lymphoma 7B, BCL 7B, BCL7B_HUMAN.
Background: BCL7B shows high homology to the BCL7A protein, which is known to be directly involved in a complex chromosomal translocation in Burkitt lymphoma cell lines. The specific function of BCL7B has not yet been determined. However, it may play a role in lung tumor development or progression. The BCL7B gene is located at a chromosomal region commonly deleted in the congenital disorder, Williams syndrome.
- ID gène
- 9275
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