ODF3B anticorps (Biotin)

N° du produit ABIN1402333

Détail du produit anti-ODF3B anticorps (Biotin)

Antigène: ODF3B (Outer Dense Fiber of Sperm Tails 3B (ODF3B))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ODF3B 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 ODF3B

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 ODF3B

Antigène: ODF3B (Outer Dense Fiber of Sperm Tails 3B (ODF3B))

Autre désignation: ODF3B (ODF3B Produits)

Synonymes: anticorps ODF3L3, anticorps 2010001J22Rik, anticorps RGD1564322, anticorps fj19d04, anticorps odf3l, anticorps si:dkeyp-1h4.4, anticorps wu:fj19d04, anticorps zgc:63985, anticorps outer dense fiber of sperm tails 3B, anticorps ODF3B, anticorps Odf3b, anticorps odf3b

Sujet:

Synonyms: ODF3B, ODF3B_HUMAN, Odf3l3, Outer dense fiber of sperm tails 3B, Outer dense fiber protein 3-like protein 3, Outer dense fiber protein 3B.

Background: ODF3B, also known as ODF3L3 (outer dense fiber protein 3-like protein 3), is a 253 amino acid protein belonging to the ODF3 family. Existing as two isoforms produced by alternative splicing, ODF3B contains one DUF1309 repeat. The gene that encodes ODF3B maps to human chromosome 22, which 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.