GTX66528
GLP antibody
Cannot supply to this region.
- SKU:
- GTX66528
- Additional Names:
- euchromatic histone lysine methyltransferase 1 , EHMT1-IT1 , EUHMTASE1 , Eu-HMTase1 , FP13812 , GLP , GLP1 , KLEFS1 , KMT1D
- Application:
- WB
- Physical State:
- Liquid
- Species Reactivity:
- Human
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Supplier:
- Genetex
- Host:
- Rabbit
- Reactivities:
- Human, Mouse, Rat
- Buffer:
- PBS, 50% Glycerol, 0.02% Sodium azide.
- Immunogen:
- Recombinant funsion protein containing a sequence corresponding to amino acids 1-260 of human EHMT1 (NP_079033.4).
- Uniprot:
- Q9H9B1
- Synonyms:
- EHMT1 intronic transcript 1;EHMT1-IT1;Eu-HMTase1;euchromatic histone-lysine N-methyltransferase 1;EUHMTASE1;FP13812;G9a-like protein 1;GLP;GLP1;H3-K9-HMTase 5;histone H3-K9 methyltransferase 5;histone-lysine N-methyltransferase EHMT1;histone-lysine N-methyltransferase, H3 lysine-9 specific 5;KLEFS1;KMT1D;lysine N-methyltransferase 1D
- Extra Details:
- The protein encoded by this gene is a histone methyltransferase that methylates the lysine-9 position of histone H3. This action marks the genomic region packaged with these methylated histones for transcriptional repression. This protein may be involved in the silencing of MYC- and E2F-responsive genes and therefore could play a role in the G0/G1 cell cycle transition. Defects in this gene are a cause of chromosome 9q subtelomeric deletion syndrome (9q-syndrome, also known as Kleefstra syndrome). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2017]
- Shipping Conditions:
- Blue Ice