SOHLH1 antibody (AA 51-118) (Biotin)

Catalog No. ABIN1701551

The Rabbit Polyclonal anti-SOHLH1 antibody has been validated for WB, ELISA, IHC (p) and IHC (fro). It is suitable to detect SOHLH1 in samples from Human.

Quick Overview for SOHLH1 antibody (AA 51-118) (Biotin) (ABIN1701551)

Target: SOHLH1 (Spermatogenesis and Oogenesis Specific Basic Helix-Loop-Helix 1 (SOHLH1))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SOHLH1 antibody is conjugated to Biotin

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

Product Details anti-SOHLH1 Antibody (Biotin)

Binding Specificity: AA 51-118

Predicted Reactivity: Human,Mouse,Rat,Cow,Pig,Horse

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human Sohlh1

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

Restrictions: For Research Use only

Handling

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.

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

Storage Comment: Store at -20°C for 12 months.

Expiry Date: 12 months

Target Details for SOHLH1

Target: SOHLH1 (Spermatogenesis and Oogenesis Specific Basic Helix-Loop-Helix 1 (SOHLH1))

Alternative Name: Sohlh1

Background:

Synonyms: GM110, Helix Loop Helix Protein TOHLH1, Sohlh1, SOLH1_HUMAN, Spermatogenesis- and oogenesis-specic basic helix-loop-helix-containing protein 1, TOHLH1.

Background: SOHLH1 is a 328 amino acid protein that localizes to both the nucleus and the cytoplasm and contains one bHLH domain through which it may function as a transcription factor during oogenesis and spermatogenesis. The gene encoding SOHLH1 maps to human chromosome 9, which houses over 900 genes and comprises nearly 4 % of the human genome. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster.

Gene ID: 402381