GTF2H2 MaxPab rabbit polyclonal antibody (D01)
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Specifications
Product Description
Rabbit polyclonal antibody raised against a full-length human GTF2H2 protein.
Immunogen
GTF2H2 (NP_001506.1, 1 a.a. ~ 395 a.a) full-length human protein.
Sequence
MDEEPERTKRWEGGYERTWEILKEDESGSLKATIEDILFKAKRKRVFEHHGQVRLGMMRHLYVVVDGSRTMEDQDLKPNRLTCTLKLLEYFVEEYFDQNPISQIGIIVTKSKRAEKLTELSGNPRKHITSLKKAVDMTCHGEPSLYNSLSIAMQTLKHMPGHTSREVLIIFSSLTTCDPSNIYDLIKTLKAAKIRVSVIGLSAEVRVCTVLARETGGTYHVILDESHYKELLTHHVSPPPASSSSECSLIRMGFPQHTIASLSDQDAKPSFSMAHLDGNTEPGLTLGGYFCPQCRAKYCELPVECKICGLTLVSAPHLARSYHHLFPLDAFQEIPLEEYNGERFCYGCQGELKDQHVYVCAVCQNVFCVDCDVFVHDSLHCCPGCIHKIPAPSGV
Host
Rabbit
Reactivity
Human
Quality Control Testing
Antibody reactive against mammalian transfected lysate.
Storage Buffer
No additive
Storage Instruction
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
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Applications
Western Blot (Transfected lysate)
Western Blot analysis of GTF2H2 expression in transfected 293T cell line (H00002966-T02) by GTF2H2 MaxPab polyclonal antibody.
Lane 1: GTF2H2 transfected lysate(44.4 KDa).
Lane 2: Non-transfected lysate.
Immunoprecipitation
Immunoprecipitation of GTF2H2 transfected lysate using anti-GTF2H2 MaxPab rabbit polyclonal antibody and Protein A Magnetic Bead, and immunoblotted with GTF2H2 MaxPab mouse polyclonal antibody (B01) (H00002966-B01). -
Gene Info — GTF2H2
Entrez GeneID
2966GeneBank Accession#
NM_001515.2Protein Accession#
NP_001506.1Gene Name
GTF2H2
Gene Alias
BTF2, BTF2P44, MGC102806, T-BTF2P44, TFIIH
Gene Description
general transcription factor IIH, polypeptide 2, 44kDa
Omim ID
601748Gene Ontology
HyperlinkGene Summary
This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. This gene is within the telomeric copy of the duplication. Deletion of this gene sometimes accompanies deletion of the neighboring SMN1 gene in spinal muscular atrophy (SMA) patients but it is unclear if deletion of this gene contributes to the SMA phenotype. This gene encodes the 44 kDa subunit of RNA polymerase II transcription initiation factor IIH which is involved in basal transcription and nucleotide excision repair. Transcript variants for this gene have been described, but their full length nature has not been determined. A second copy of this gene within the centromeric copy of the duplication has been described in the literature. It is reported to be different by either two or four base pairs; however, no sequence data is currently available for the centromeric copy of the gene. [provided by RefSeq
Other Designations
general transcription factor IIH, polypeptide 2 (44kD subunit)|general transcription factor IIH, polypeptide 2, 44kD subunit
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Interactomes
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Pathways
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Diseases
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