Anoctamin 5 antibody (C-Term)

Catalog No. ABIN499159

Product Details anti-Anoctamin 5 Antibody

Target: Anoctamin 5 (ANO5)

Binding Specificity: AA 798-828, C-Term

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Anoctamin 5 antibody is un-conjugated

Application: Western Blotting (WB), Enzyme Immunoassay (EIA)

Specificity: Recognizes ANO5 (C-term).

Purification: Protein A Chromatography followed by peptide affinity purification

Immunogen: Synthetic peptide -KLH conjugated between 798~828 amino acids from the C-terminal region of Human ANO5. Genename: ANO5

Isotype: Ig Fraction

Application Details

Application Notes: ELISA: 1/1,000. Western blotting: 1/100-1/500.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user.

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.25 mg/mL

Buffer: PBS with 0.09 % (W/V) Sodium Azide as preservative

Preservative: Sodium azide

Precaution of Use: This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Handling Advice: Avoid repeated freezing and thawing.

Storage: 4 °C/-20 °C

Storage Comment: Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Target Details for Anoctamin 5

Target: Anoctamin 5 (ANO5)

Alternative Name: ANO5 (ANO5 Products)

Synonyms: gdd1 antibody, tmem16e antibody, MGC82557 antibody, TMEM16E antibody, ano5 antibody, si:dkey-261m9.4 antibody, GDD1 antibody, LGMD2L antibody, 9330162L24 antibody, Gdd1 antibody, Tmem16e antibody, anoctamin 5 L homeolog antibody, anoctamin 5 antibody, anoctamin 5a antibody, ano5.L antibody, ANO5 antibody, ano5a antibody, ano5 antibody, Ano5 antibody

Background: ANO5 is a member of the anoctamin family of transmembrane proteins. This protein is likely a calcium activated chloride channel. Defects in ANO5 are the cause of gnathodiaphyseal dysplasia (GDD), also known as osteogenesis imperfecta with unusual skeletal lesions or gnathodiaphyseal sclerosis. GDD is a rare skeletal syndrome characterized by bone fragility, sclerosis of tubular bones, and cemento-osseous lesions of the jawbone. Patients experience frequent bone fractures caused by trivial accidents in childhood, however the fractures heal normally without bone deformity. The jaw lesions replace the tooth-bearing segments of the maxilla and mandible with fibrous connective tissues, including various amounts of cementum-like calcified mass, sometimes causing facial deformities. Patients also have a propensity for jaw infection and often suffer from purulent osteomyelitis-like symptoms, such as swelling of and pus discharge from the gums, mobility of the teeth, insufficient healing after tooth extraction and exposure of the lesions into the oral cavity.Synonyms: Anoctamin-5, GDD1, Gnathodiaphyseal dysplasia 1 protein, TMEM16E, Transmembrane 16E

Gene ID: 203859

NCBI Accession: NP_001136121

UniProt: Q75V66