IFFO2 Antibody (C-term) Blocking Peptide
€363.00
In stock
SKU
AC-BP16608b
Background:
IFFO2 (intermediate filament family orphan 2) is 517 amino acid protein that is encoded by a gene mapping to human chromosome 1p36.13 and mouse chromosome 4 D3. Human chromosome 1 spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson聮s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.
Other Names:
Intermediate filament family orphan 2, IFFO2
Gene Name: IFFO2
Gene ID: 126917
Primary Accession: Q5TF58
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
IFFO2 (intermediate filament family orphan 2) is 517 amino acid protein that is encoded by a gene mapping to human chromosome 1p36.13 and mouse chromosome 4 D3. Human chromosome 1 spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson聮s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.
Other Names:
Intermediate filament family orphan 2, IFFO2
Gene Name: IFFO2
Gene ID: 126917
Primary Accession: Q5TF58
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
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