C5orf35 anticorps (AA 1-100) (Biotin)

N° du produit ABIN1700136

Cet anticorps anti-C5orf35 est un anticorps Lapin Polyclonal détectant C5orf35 dans WB, ELISA, IHC (p) et IHC (fro). Adapté pour Humain.

Aperçu rapide pour C5orf35 anticorps (AA 1-100) (Biotin) (ABIN1700136)

Antigène: C5orf35 (Chromosome 5 Open Reading Frame 35 (C5orf35))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C5orf35 est conjugé à/à la Biotin

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Détail du produit anti-C5orf35 anticorps (Biotin)

Épitope: AA 1-100

Homologie: Human,Dog

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C5orf35

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

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 for 12 months.

Date de péremption: 12 months

Détails sur C5orf35

Antigène: C5orf35 (Chromosome 5 Open Reading Frame 35 (C5orf35))

Autre désignation: C5orf35

Sujet:

Synonyms: C5orf35 chromosome 5 open reading frame 35, Chromosome 5 open reading frame 35, Hypothetical protein LOC133383, MGC33648, Uncharacterized protein C5orf35, SET domain-containing protein 9, SETD9_HUMAN.

Background: C5orf35 is a With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6 % of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The C5orf35 gene product has been provisionally designated C5orf35 pending further characterization.

ID gène: 133383