CCDC102B anticorps (AA 50-130)
Aperçu rapide pour CCDC102B anticorps (AA 50-130) (ABIN7214022)
Antigène
Voir toutes CCDC102B AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 50-130
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Fonction
- CCDC102B Polyclonal Antibody
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Specificité
- CCDC102B Polyclonal Antibody detects endogenous levels of CCDC102B protein.
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Purification
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen
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Immunogène
- Synthesized peptide derived from the Internal region of human CCDC102B at AA range: 50-130
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Isotype
- IgG
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Indications d'application
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), IHC-P (1:100-1:300), ELISA (1:40000). Not yet tested in other applications.
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Commentaires
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Primary Antibody
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 mg/mL
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Buffer
- PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.
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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Stock
- -20 °C
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Stockage commentaire
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
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- CCDC102B (Coiled-Coil Domain Containing 102B (CCDC102B))
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Autre désignation
- CCDC102B
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Sujet
- Rabbit Anti-CCDC102B Polyclonal Antibody,CCDC102B, C18orf14, Coiled-coil domain-containing protein 102B,CCDC102B (coiled-coil domain containing 102B), also known as AN, ACY1L or HsT1731, is a 513 amino acid protein that exists as three alternatively spliced isoforms. Widely expressed and found in multiple CNV (copy-number variant) regions, CCDC102B contains the deletion breakpoint of a maternally inherited deletion, which is 2.7Mb in size, and maps to human chromosome 18q22.1. CCDC102B may play a role in the pathogenesis of diaphragmatic hernia, microphthalmia, colorectal carcinoma and schizophrenia. Encoding over 300 genes, chromosome 18 contains about 76 million bases. Translocation between chromosomes 18 and 14 is the most common translocation in cancers and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18.,Coiled-coil domain-containing protein 102B
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Poids moléculaire
- observerd band 60kDa
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ID gène
- 79839
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UniProt
- Q68D86
Antigène
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