C4ORF17 anticorps (AA 121-220) (Biotin)

N° du produit ABIN1701002

L’anticorps Lapin Polyclonal anti-C4ORF17 a été validé pour WB, ELISA, IHC (fro) et IHC (p). Il convient pour détecter C4ORF17 dans des échantillons de Humain.

Aperçu rapide pour C4ORF17 anticorps (AA 121-220) (Biotin) (ABIN1701002)

Antigène: C4ORF17 (Chromosome 4 Open Reading Frame 17 (C4ORF17))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C4ORF17 est conjugé à/à la Biotin

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

Détail du produit anti-C4ORF17 anticorps (Biotin)

Épitope: AA 121-220

Homologie: Human,Mouse,Rat,Dog,Cow,Sheep

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C4orf17

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 C4ORF17

Antigène: C4ORF17 (Chromosome 4 Open Reading Frame 17 (C4ORF17))

Autre désignation: C4orf17

Sujet:

Synonyms: C4orf17, CD017_HUMAN, Chromosome 4 open reading frame 17, Uncharacterized protein C4orf17.

Background: C4orf17 (chromosome 4 open reading frame 17) is a 359 amino acid protein encoded by a gene that maps to human chromosome 4. Human chromosome 4 represents approximately 6 % of the human genome and contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded by a gene that is located on chromosome 4, and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.