Sp1 (Acetyl Lys703) Rabbit Polyclonal Antibody, 100ul Endonucleases & Exonucleases also known as hereditary hyperekplexia

also known as hereditary hyperekplexia or congenital stiff-person syndrome

followed by release from cell membranes [PMID: 10748068]

This gene is clustered with related family members on chromosome 5q33

This gene encodes a member of the phosphatase and actin regulator protein family

the number of DAZ repeats is variable and there are several variations in the sequence of the DAZ repeat

Sp1 (Acetyl Lys703) Rabbit Polyclonal Antibody, 100ul Endonucleases & Exonucleases also known as hereditary hyperekplexiaBinds to GC box promoters elements and selectively activates mRNA synthesis from genes that contain functional recognition sites. Can interact with G C rich motifs from serotonin receptor promoter. PTM: O glycosylated; contains N acetylglucosamine side chains. Belongs to the Sp1 C2H2 type zinc finger protein family. Contains 3 C2H2 type zinc fingers. subunit: Interacts with ATF7IP ATF7IP2 POGZ HCFC1 AATF and PHC2. Interacts with varicella zoster virus