C9orf25 anticorps (AA 1-100) (Cy5)

N° du produit ABIN1704089

Détail du produit anti-C9orf25 anticorps (Cy5)

Antigène: C9orf25 (Chromosome 9 Open Reading Frame 25 (C9orf25))

Épitope: AA 1-100

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C9orf25 est conjugé à/à la Cy5

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

Homologie: Human,Mouse,Rat,Sheep,Horse,Chicken

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C9orf25

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 C9orf25

Antigène: C9orf25 (Chromosome 9 Open Reading Frame 25 (C9orf25))

Autre désignation: C9orf25 (C9orf25 Produits)

Synonymes: anticorps C9orf25, anticorps bA573M23.5, anticorps C15H9orf25, anticorps 2310028H24Rik, anticorps fam219a, anticorps zgc:101028, anticorps family with sequence similarity 219 member A, anticorps family with sequence similarity 219, member A, anticorps family with sequence similarity 219, member Aa, anticorps FAM219A, anticorps Fam219a, anticorps fam219aa

Sujet:

Synonyms: bA573M23.5, C9orf25, Chromosome 9 open reading frame 25, F219A_HUMAN, FLJ39031, Hypothetical protein LOC203259, Uncharacterized protein C9orf25.

Background: C9orf25 (chromosome 9 open reading frame 25) is a 185 amino acid protein that exists as seven alternatively spliced isoforms that are encoded by a gene located on human chromosome 9. Chromosome 9 consists of about 145 million bases, represents 4 % of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.

ID gène: 203259