FAM82A1 anticorps (AA 261-360)

N° du produit ABIN1385917

Cet anticorps Lapin Polyclonal détecte spécifiquement FAM82A1 dans ELISA, IF (cc), IF (p), IHC (fro) et IHC (p). Il présente une réactivité envers Humain.

Aperçu rapide pour FAM82A1 anticorps (AA 261-360) (ABIN1385917)

Antigène: FAM82A1 (RMDN2) (Regulator of Microtubule Dynamics 2 (RMDN2))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FAM82A1 est non-conjugé

Application: ELISA, Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-FAM82A1 anticorps

Épitope: AA 261-360

Homologie: Human,Mouse,Rat,Dog,Pig,Horse

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human FAM82A1

Isotype: IgG

Information d'application

Indications d'application: ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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: 4 °C,-20 °C

Stockage commentaire: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Détails sur FAM82A1

Antigène: FAM82A1 (RMDN2) (Regulator of Microtubule Dynamics 2 (RMDN2))

Autre désignation: Fam82a1

Sujet:

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.