EHMT1 antibody (AA 25-75)

Catalog No. ABIN7453694

Product Details anti-EHMT1 Antibody

Target: EHMT1 (Euchromatic Histone-Lysine N-Methyltransferase 1 (EHMT1))

Binding Specificity: AA 25-75

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This EHMT1 antibody is un-conjugated

Application: Western Blotting (WB), Immunoprecipitation (IP), Immunohistochemistry (Formalin-fixed Paraffin-embedded Sections) (IHC (fp))

Purpose: Rabbit anti-EHMT1 Antibody, Affinity Purified

Purification: Affinity Purified

Immunogen: between AA 25 and 75

Isotype: IgG

Application Details

Application Notes:

IHC: 1:100 - 1:500. Epitope retrieval with citrate buffer pH 6.0 is recommended for FFPE tissue sections.

IP: 2 - 5 μg/mg lysate

WB: 1:2,000 - 1:10,000

Restrictions: For Research Use only

Handling

Concentration: 200 μg/mL

Buffer: Tris-buffered Saline containing 0.1 % BSA and 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: 4 °C

Expiry Date: 12 months

Target Details for EHMT1

Target: EHMT1 (Euchromatic Histone-Lysine N-Methyltransferase 1 (EHMT1))

Alternative Name: EHMT1 (EHMT1 Products)

Synonyms: EUHMTASE1 antibody, Eu-HMTase1 antibody, FP13812 antibody, GLP antibody, GLP1 antibody, KMT1D antibody, bA188C12.1 antibody, EHMT1 antibody, G9a antibody, 9230102N17Rik antibody, D330003E03 antibody, mKIAA1876 antibody, bZ1O1.6 antibody, si:rp71-1o1.6 antibody, zgc:136244 antibody, euchromatic histone lysine methyltransferase 1 antibody, histone-lysine N-methyltransferase EHMT2 antibody, euchromatic histone-lysine N-methyltransferase 1 antibody, euchromatic histone methyltransferase 1 antibody, euchromatic histone-lysine N-methyltransferase 1a antibody, EHMT1 antibody, Ehmt1 antibody, LOC100121084 antibody, ehmt1 antibody, ehmt1a antibody

Background: Background: Euchromatic histone-lysine N-methyltransferase 1 (EHMT1) is a histone methyltransferase that catalyzes the methylation of lysine-9 of histone H3 (H3-K9). H3-K9 histone methylation is restricted to euchromatin and functions to epigenetically silence gene transcription. Loss of function mutations in EHMT1 cause the 9q34 subtelomeric deletion syndrome, a syndrome characterized by severe mental retardation, hypotonia, brachy(micro)cephaly, heart defects, and distinct facial anomalies.

Gene ID: 79813

NCBI Accession: NP_079033

UniProt: Q9H9B1