GFI1B Polyclonal Antibody

Background:
This gene encodes a zinc-finger containing transcriptional regulator that is primarily expressed in cells of hematopoietic lineage. The encoded protein complexes with numerous other transcriptional regulatory proteins including GATA-1, runt-related transcription factor 1 and histone deacetylases to control expression of genes involved in the development and maturation of erythrocytes and megakaryocytes. Mutations in this gene are the cause of the autosomal dominant platelet disorder, platelet-type bleeding disorder-17. Alternate splicing results in multiple transcript variants.GFI1B (Growth Factor Independent 1B Transcriptional Repressor) is a Protein Coding gene. Diseases associated with GFI1B include Bleeding Disorder, Platelet-Type, 17 and Gray Platelet Syndrome. Among its related pathways are NF-kappaB Signaling. GO annotations related to this gene include RNA polymerase II transcription factor binding. An important paralog of this gene is GFI1.

Research Area: Cardiovascular, Epigenetics and Nuclear Signaling

Synonyms:
GFI 1B, gfi1b, GFI1B protein, GFI1B, Growth factor independent 1B protein, Growth factor independent 1B transcription repressor, Growth factor independent protein 1B, OTTHUMP00000022443, OTTHUMP00000022444, OTTHUMP000000235527, Potential regulator of CDKN1A, Potential regulator of CDKN1A translocated in CML, Translocated in CML, Zinc finger protein Gfi-1b

Immunogen: Synthetic peptide of human GFI1B

Swissprot: Q5VTD9
Gene Accession: NP004179

Purification Method: Antigen affinity purification

Buffer: PBS with 0.05% NaN3 and 40% Glycerol, pH7.4

Concentration: 0.72 mg/mL
Dilution: IHC 1:40-1:200, ELISA 1:5000-1:10000

Storage:
Store at -20°C. Avoid freeze / thaw cycles.