|Western Blot (WB)||1:500-1:1000|
|Tested Species reactivity||Human, Rat|
|Host / Isotype||Rabbit / IgG|
|Immunogen||A synthetic peptide corresponding to residues in human COL26A1|
|Purification||Antigen affinity chromatography|
|Storage buffer||PBS with 50% glycerol|
|Contains||0.1% sodium azide|
|Storage conditions||Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.|
This antibody detects endogenous protein at a molecular weight of 45 and 55 kDa.
Purity is >95% by SDS-PAGE.
COL26A1 (EMID2) is a 441 amino acid protein encoded by a gene mapping to human chromosome 7. Chromosome 7 is approximately 158 milllion bases long, encodes over 1,000 genes and makes up about 5% of the human genome. Chromosome 7 has been linked to osteogenesis imperfecta, Pendred syndrome, lissencephaly, citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers, and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Alpha-1 type XXVI collagen; COL26A1; Collagen alpha-1(XXVI) chain; collagen, type XXVI, alpha 1; EMI domain containing 2; EMI domain-containing protein 2; EMID2; Emilin and multimerin domain-containing protein 2; EMU2
Gene Aliases: COL26A1; EMI6; EMID2; EMU2; SH2B
UniProt ID: (Human) Q96A83
Entrez Gene ID: (Human) 136227
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