CHCHD5 anticorps (AA 21-110) (FITC)

N° du produit ABIN890366

L’anticorps anti-CHCHD5 Polyclonal produit chez le Lapin a été validé pour IF (cc) et IF (p). Il convient pour la détection de CHCHD5 dans des échantillons provenant de Humain. }

Aperçu rapide pour CHCHD5 anticorps (AA 21-110) (FITC) (ABIN890366)

Antigène: CHCHD5 (Coiled-Coil-Helix-Coiled-Coil-Helix Domain Containing 5 (CHCHD5))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CHCHD5 est conjugé à/à la FITC

Application: Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Détail du produit anti-CHCHD5 anticorps (FITC)

Épitope: AA 21-110

Homologie: Human,Mouse,Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human CCDC99

Isotype: IgG

Information d'application

Indications d'application: 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: 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

Détails sur CHCHD5

Antigène: CHCHD5 (Coiled-Coil-Helix-Coiled-Coil-Helix Domain Containing 5 (CHCHD5))

Autre désignation: CHCHD5

Sujet:

Synonyms: C2orf9, CHCH5_HUMAN, CHCHD5, chromosome 2 open reading frame, Coiled coil helix coiled coil helix domain containing 5, Coiled-coil-helix-coiled-coil-helix domain-containing protein 5, FLJ39671, MGC11104.

Background: CHCHD5 is a 110 amino acid protein that contains one CHCH domain. The gene encoding CHCHD5 maps to human chromosome 2, which 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.

ID gène: 84269