SIM1 antibody (AA 1-30)

Catalog No. ABIN7869106

The Rabbit Polyclonal anti-SIM1 antibody (ABIN7869106) specifically detects SIM1 in WB and IHC (p). The antibody is reactive with Human samples.

Quick Overview for SIM1 antibody (AA 1-30) (ABIN7869106)

Target: SIM1 (Single-Minded Homolog 1 (SIM1))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SIM1 antibody is un-conjugated

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

Product Details anti-SIM1 Antibody

Binding Specificity: AA 1-30

Purpose: Single-minded homolog 1 Antibody / SIM1

Purification: Antigen affinity purified

Immunogen: A portion of amino acids 1-30 from the human protein was used as the immunogen for the Single-minded homolog 1 antibody.

Isotype: Ig Fraction

Application Details

Application Notes: The stated application concentrations are suggested starting points. Titration of the Single-minded homolog 1 antibody may be required due to differences in protocols and secondary/substrate sensitivity.

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: In 1X PBS, pH 7.4, with 0.09 % sodium azide

Preservative: Sodium azide

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

Storage: -20 °C

Storage Comment: Aliquot the Single-minded homolog 1 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Target Details for SIM1

Target: SIM1 (Single-Minded Homolog 1 (SIM1))

Alternative Name: Single-minded homolog 1

Background: SIM1 and SIM2 genes are Drosophila single-minded (sim) gene homologs. SIM1 transcript was detected only in fetal kidney out of various adult and fetal tissues tested. Since the sim gene plays an important role in Drosophila development and has peak levels of expression during the period of neurogenesis,it was proposed that the human SIM gene is a candidate for involvement in certain dysmorphic features (particularly the facial and skull characteristics), abnormalities of brain development, and/or mental retardation of Down syndrome.

UniProt: P81133