C4orf33 anticorps

N° du produit ABIN1385966

L’anticorps Lapin Polyclonal anti-C4orf33 a été validé pour WB, IF (p) et IHC (p). Il convient pour détecter C4orf33 dans des échantillons de Humain, Souris et Rat.

Aperçu rapide pour C4orf33 anticorps (ABIN1385966)

Antigène: C4orf33 (Chromosome 4 Open Reading Frame 33 (C4orf33))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C4orf33 est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-C4orf33 anticorps

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C4orf33

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
IHC-P 1:200-400
IF(IHC-P) 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 C4orf33

Antigène: C4orf33 (Chromosome 4 Open Reading Frame 33 (C4orf33))

Autre désignation: C4orf33

Sujet:

Synonyms: C4orf33, C4orf33 chromosome 4 open reading frame 33, CD033_HUMAN, UPF0462 protein C4orf33.

Background: C4orf33 is a 199 amino acid protein that is 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 located on chromosome 4. FGFR-3 is also encoded by a gene that maps to human 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.

ID gène: 132321