ATM polyclonal, anti-human, mouse antibody
€295.00
In stock
SKU
AC-ABV10627-100
Catalog Number: AC-ABV10627-100
Size: 100 µl
Host: Rabbit IgG
Applications: WB, IP
Datasheet
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Size: 100 µl
Host: Rabbit IgG
Applications: WB, IP
Datasheet
Request Information
Background:
The phosphatidylinositol kinase (PIK) family members fall into two distinct subgroups. The first subgroup contains proteins such as the PI 3- and PI 4-kinases and the second group comprises the PIK-related kinases. The PIK-related kinases include Atm, DNA-PKCS and FRAP. These proteins have in common a region of homology at their carboxy termini that is not present in the PI 3- and PI 4-kinases. All of the members of the PIK-related kinases are also larger than 270 kDa. The Atm gene is mutated in the autosomal recessive disorder ataxia telangiectasia (AT), which is characterized by cerebellar degeneration (ataxia) and the appearance of dilated blood vessels (telangiectases) in the conjunctivae of the eyes. AT cells are hypersensitive to ionizing radiation, impaired in mediating the inhibition of DNA synthesis and they display delays in p53 induction.
Other Names:
AT complementation group A, AT complementation group C, AT complementation group D, AT complementation group E , ATE, ATDC
Primary Accession: Q13315
Gene Name: ATM
Gene ID: 472
Concentration (mg/ml): 0.5 mg/ml
The phosphatidylinositol kinase (PIK) family members fall into two distinct subgroups. The first subgroup contains proteins such as the PI 3- and PI 4-kinases and the second group comprises the PIK-related kinases. The PIK-related kinases include Atm, DNA-PKCS and FRAP. These proteins have in common a region of homology at their carboxy termini that is not present in the PI 3- and PI 4-kinases. All of the members of the PIK-related kinases are also larger than 270 kDa. The Atm gene is mutated in the autosomal recessive disorder ataxia telangiectasia (AT), which is characterized by cerebellar degeneration (ataxia) and the appearance of dilated blood vessels (telangiectases) in the conjunctivae of the eyes. AT cells are hypersensitive to ionizing radiation, impaired in mediating the inhibition of DNA synthesis and they display delays in p53 induction.
Other Names:
AT complementation group A, AT complementation group C, AT complementation group D, AT complementation group E , ATE, ATDC
Primary Accession: Q13315
Gene Name: ATM
Gene ID: 472
Concentration (mg/ml): 0.5 mg/ml
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