TCEAL8 polyclonal, anti-human, mouse, rat
€305.00
In stock
SKU
BS60497
Background:
TCEAL8 (transcription elongation factor A protein-like 8), also known as transcription elongation factor S-II protein-like 8, is a 117 amino acid nuclear protein that belongs to the TFS-II family and the TFA subfamily, and may be involved in transcriptional regulation. The gene that encodes TCEAL8 contains approximately 2,209 bases and maps to human chromosome Xq22.1. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of a X and Y chromosome leads to normal male development while two copies of X leads to normal female development. There are a number of conditions related to an unusual number and combination of sex chromosomes being inherited, including Turner’s syndrome, Klinefelter’s syndrome and Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.
Alternative Name:
Transcription elongation factor A protein-like 8, TCEA-like protein 8, Transcription elongation factor S-II protein-like 8, TCEAL8
Application Dilution: WB: 1:500~1:1000
Specificity: TCEAL8 polyclonal antibody detects endogenous levels of TCEAL8 protein.
Immunogen:
A synthetic peptide corresponding to residues in Human TCEAL8.
MW: ~ 14 kDa
Swis Prot.: Q8IYN2
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:
1 mg/ml in Phosphate buffered saline (PBS) with 15 mM sodium azide, approx. pH 7.2.
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.
TCEAL8 (transcription elongation factor A protein-like 8), also known as transcription elongation factor S-II protein-like 8, is a 117 amino acid nuclear protein that belongs to the TFS-II family and the TFA subfamily, and may be involved in transcriptional regulation. The gene that encodes TCEAL8 contains approximately 2,209 bases and maps to human chromosome Xq22.1. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of a X and Y chromosome leads to normal male development while two copies of X leads to normal female development. There are a number of conditions related to an unusual number and combination of sex chromosomes being inherited, including Turner’s syndrome, Klinefelter’s syndrome and Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.
Alternative Name:
Transcription elongation factor A protein-like 8, TCEA-like protein 8, Transcription elongation factor S-II protein-like 8, TCEAL8
Application Dilution: WB: 1:500~1:1000
Specificity: TCEAL8 polyclonal antibody detects endogenous levels of TCEAL8 protein.
Immunogen:
A synthetic peptide corresponding to residues in Human TCEAL8.
MW: ~ 14 kDa
Swis Prot.: Q8IYN2
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:
1 mg/ml in Phosphate buffered saline (PBS) with 15 mM sodium azide, approx. pH 7.2.
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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