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Rabbit Anti-ZNF778/FITC Conjugated antibody
background:
The protein encoded by this gene is a member of the krueppel C2H2-type zinc-finger protein family, and it contains one KRAB domain and eighteen C2H2-type zinc fingers. This gene is a candidate gene for autism and variable cognitive impairment in the 16q24.3 microdeletion syndrome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2011]
Function:
FLJ31875 belongs to the krueppel C2H2 type zinc finger protein family. It contains 19 C2H2 type zinc fingers and 1 KRAB domain. FLJ31875 may be involved in transcriptional regulation. There are 2 named isoforms of 78 and 74 kDa.
Subcellular Location:
Nuclear
Similarity:
Belongs to the krueppel C2H2-type zinc-finger protein family.
Contains 18 C2H2-type zinc fingers.
Contains 1 KRAB domain.
Database links:
Entrez Gene: 19764 Human
SwissProt: Q96MU6 Human
Unigene: 647385 Human
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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