C22orf25 anticorps (AA 25-75) (Biotin)

N° du produit ABIN1405777

Détail du produit anti-C22orf25 anticorps (Biotin)

Antigène: C22orf25 (Chromosome 22 Open Reading Frame 25 (C22orf25))

Épitope: AA 25-75

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C22orf25 est conjugé à/à la Biotin

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

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C22orf25

Isotype: IgG

Information d'application

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

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 C22orf25

Antigène: C22orf25 (Chromosome 22 Open Reading Frame 25 (C22orf25))

Autre désignation: C22orf25 (C22orf25 Produits)

Synonymes: anticorps c22orf25, anticorps MGC88919, anticorps C22orf25, anticorps TANGO2, anticorps C17H22orf25, anticorps transport and golgi organization 2 homolog L homeolog, anticorps transport and golgi organization 2 homolog, anticorps transport and golgi organization 2 homolog (Drosophila), anticorps tango2.L, anticorps tango2, anticorps TANGO2

Sujet:

Synonyms: Uncharacterized protein C22orf25, chromosome 22 open reading frame 25, DKFZp 761 P 1121, Hypothetical protein LOC128989, TNG2_HUMAN, TANGO2, Transport and Golgi organization protein 2 homolog.

Background: Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia. The C22orf25 gene product has been provisionally designated C22orf25 pending further characterization.

ID gène: 128989

UniProt: Q6ICL3