C7ORF57 anticorps (AA 161-260) (Biotin)
Aperçu rapide pour C7ORF57 anticorps (AA 161-260) (Biotin) (ABIN1700845)
Antigène
Reactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 161-260
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Réactivité croisée
- Rat
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Homologie
- Human,Mouse,Cow,Sheep,Horse
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Purification
- Purified by Protein A.
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Immunogène
- KLH conjugated synthetic peptide derived from human C7orf57
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Isotype
- IgG
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anti-Chromosome 7 Open Reading Frame 57 (C7ORF57) (AA 161-260) antibody
C7ORF57 Reactivité: Rat IF (cc), IF (p), ELISA, IHC (fro), IHC (p), ICC Hôte: Lapin Polyclonal unconjugated
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Indications d'application
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IHC-P 1:200-400
IHC-F 1:100-500 -
Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 μg/μL
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Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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Agent conservateur
- ProClin
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Précaution d'utilisation
- This product contains ProClin: 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
- Store at -20°C for 12 months.
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Date de péremption
- 12 months
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- C7ORF57 (Chromosome 7 Open Reading Frame 57 (C7ORF57))
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Autre désignation
- C7orf57
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Sujet
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Synonyms: C7orf57, CG057_HUMAN, Chromosome 7 open reading frame 57, Uncharacterized protein C7orf57.
Background: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf57 gene product has been provisionally designated C7orf57 pending further characterization.
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ID gène
- 136288
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UniProt
- Q8NEG2
Antigène
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