FAM82A1 anticorps (AA 261-360) (AbBy Fluor® 680)
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- Antigène Tous les produits FAM82A1 (RMDN2)
- FAM82A1 (RMDN2) (Regulator of Microtubule Dynamics 2 (RMDN2))
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Épitope
- AA 261-360
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp FAM82A1 est conjugé à/à la AbBy Fluor® 680
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Application
- Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunofluorescence (Cultured Cells) (IF (cc))
- Homologie
- Human,Mouse,Rat,Dog,Pig,Horse
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human FAM82A1
- 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
- FAM82A1 (RMDN2) (Regulator of Microtubule Dynamics 2 (RMDN2))
- Autre désignation
- FAM82A1 (RMDN2 Produits)
- Synonymes
- anticorps FAM82A, anticorps FAM82A1, anticorps PRO34163, anticorps PYST9371, anticorps RMD-2, anticorps RMD2, anticorps RMD4, anticorps regulator of microtubule dynamics 2, anticorps RMDN2
- Sujet
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Synonyms: BLOCK18, FAM82A, Fam82a1, Family with sequence similarity 82 member A, Family with sequence similarity 82, member A1, hRMD 2, hRMD 4, hRMD-2, hRMD4, MGC33318, Microtubule associated protein, Protein FAM82A1, Regulator of microtubule dynamics, Regulator of microtubule dynamics protein 2, RMD 2, RMD-2, RMD2, RMD2_HUMAN.
Background: The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes. The FAM82A gene product has been provisionally designated FAM82A pending further characterization.
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