AMHR2 antibody (AA 18-149)

Catalog No. ABIN7092984

This Rabbit Monoclonal antibody specifically detects AMHR2 in ELISA and FACS. It exhibits reactivity toward Human.

Quick Overview for AMHR2 antibody (AA 18-149) (ABIN7092984)

Target: AMHR2 (Anti-Mullerian Hormone Receptor, Type II (AMHR2))

Reactivity: Human

Host: Rabbit

Clonality: Monoclonal

Conjugate: This AMHR2 antibody is un-conjugated

Application: ELISA, Flow Cytometry (FACS)

Clone: DM186

Product Details anti-AMHR2 Antibody

Binding Specificity: AA 18-149

Purification: Powder

Immunogen: Recombinant human AMHR2(Pro18-Leu149) (ABIN7092714) produced by using human HEK293 cells

Isotype: IgG

Application Details

Application Notes: ELISA 1/5000-10000,Flow Cyt 1/100

Restrictions: For Research Use only

Handling

Format: Lyophilized

Reconstitution: Reconstitute with deionized water

Buffer: Lyophilized from sterile PBS, pH 7.4. Normally 5 % - 8 % trehalose is added as protectants before lyophilization.,0.1 % Procline 300

Preservative: ProClin

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

Storage: -20 °C,-80 °C

Storage Comment: Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing). Lyophilized proteins are shipped at ambient temperature.

Expiry Date: 12 months

Target Details for AMHR2

Target: AMHR2 (Anti-Mullerian Hormone Receptor, Type II (AMHR2))

Alternative Name: AMHR2

Background: Synonyms:AMHR, MISR2, MISRII, MRII
Description:This gene encodes the receptor for the anti-Mullerian hormone (AMH) which, in addition to testosterone, results in male sex differentiation. AMH and testosterone are produced in the testes by different cells and have different effects. Testosterone promotes the development of male genitalia while the binding of AMH to the encoded receptor prevents the development of the mullerian ducts into uterus and Fallopian tubes. Mutations in this gene are associated with persistent Mullerian duct syndrome type II. Alternatively spliced transcript variants encoding different isoforms have been identified.

Molecular Weight: 62.8KDa