COL26A1 polyclonal, anti-human, rat
€305.00
In stock
SKU
BS60291
Background:
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.
Alternative Name:
Collagen alpha-1(XXVI) chain, Alpha-1 type XXVI collagen, EMI domain-containing protein 2, Emilin and multimerin domain-containing protein 2, Emu2, COL26A1, EMID2, EMU2
Application Dilution: WB: 1:500~1:1000
Specificity: COL26A1 polyclonal antibody detects endogenous levels of COL26A1 protein.
Immunogen:
A synthetic peptide corresponding to residues in Human COL26A1.
MW: ~ 45, 55 kDa
Swis Prot.: Q96A83
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.
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.
Alternative Name:
Collagen alpha-1(XXVI) chain, Alpha-1 type XXVI collagen, EMI domain-containing protein 2, Emilin and multimerin domain-containing protein 2, Emu2, COL26A1, EMID2, EMU2
Application Dilution: WB: 1:500~1:1000
Specificity: COL26A1 polyclonal antibody detects endogenous levels of COL26A1 protein.
Immunogen:
A synthetic peptide corresponding to residues in Human COL26A1.
MW: ~ 45, 55 kDa
Swis Prot.: Q96A83
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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