C16orf80 polyclonal, anti-human, mouse, rat
€388.00
In stock
SKU
BS8707
Background:
GTL3 (gene trap locus 3), also known as EVORF, fSAP23, C16orf80 or transcription factor IIB, is a 193 amino acid protein belonging to the UPF0468 family and may be involved in transcriptional regulation. The gene encoding GTL3 maps to human chromosome 16, which is associated with a variety of genetic disorders, encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
Alternative Name:
Cilia- and flagella-associated protein 20, Basal body up-regulated protein 22, Transcription factor IIB, CFAP20, BUG22, C16orf80
Application Dilution: WB: 1:500~1:2000, IF: 1:50~1:200
Specificity: C16orf80 polyclonal antibody detects endogenous levels of C16orf80 protein.
Immunogen:
Recombinant full length Human C16orf80.
MW: ~ 23kDa
Swis Prot.: Q9Y6A4
Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Format:
1mg/ml in PBS with 0.1% Sodium Azide, 50% Glycerol.
Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
For research use only, not for use in diagnostic procedure.
GTL3 (gene trap locus 3), also known as EVORF, fSAP23, C16orf80 or transcription factor IIB, is a 193 amino acid protein belonging to the UPF0468 family and may be involved in transcriptional regulation. The gene encoding GTL3 maps to human chromosome 16, which is associated with a variety of genetic disorders, encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
Alternative Name:
Cilia- and flagella-associated protein 20, Basal body up-regulated protein 22, Transcription factor IIB, CFAP20, BUG22, C16orf80
Application Dilution: WB: 1:500~1:2000, IF: 1:50~1:200
Specificity: C16orf80 polyclonal antibody detects endogenous levels of C16orf80 protein.
Immunogen:
Recombinant full length Human C16orf80.
MW: ~ 23kDa
Swis Prot.: Q9Y6A4
Purification & Purity:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Format:
1mg/ml in PBS with 0.1% Sodium Azide, 50% Glycerol.
Storage:
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
For research use only, not for use in diagnostic procedure.
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