SOHLH1 antibody (AA 51-118) (Cy5)

Catalog No. ABIN1705173

This anti-SOHLH1 antibody is a Rabbit Polyclonal antibody detecting SOHLH1 in WB, IF (cc) and IF (p). Suitable for Human.

Quick Overview for SOHLH1 antibody (AA 51-118) (Cy5) (ABIN1705173)

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 Cy5

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Product Details anti-SOHLH1 Antibody (Cy5)

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: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

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