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Atm Antibodies

PRODUCT NAME CATALOG # ISOTYPE EPITOPE APPLICATIONS SPECIES
Atm (H-248) Antibody sc-7230 rabbit IgG 2830-3056 (h) WB, IP, IF, ELISA m, r, h, e, c, b, p, a
Atm (2C1) Antibody sc-23921 mouse IgG1 2577-3056 (h) WB, IP, IF m, r, h
Atm (ATM 11G12) Antibody sc-53173 mouse IgG1 992-1144 (h) WB, IP, IF human
Atm (C-20) Antibody sc-1212 goat IgG C-terminus (h) WB, IP, IF, ELISA m, r, h, e, c, b, a
Atm (H-280) Antibody sc-15392 rabbit IgG 2581-2860 (h) WB, IP, IF, ELISA m, r, h, e, c, b, p
Atm (H-300) Antibody sc-28881 rabbit IgG 1-300 (h) WB, IP, IF, ELISA m, r, h, e, c, b, p
Atm (K-19) Antibody sc-1214 goat IgG C-terminus (h) WB, IP, IF, ELISA m, r, h, e, c, b, p, a
Atm (N-17) Antibody sc-1213 goat IgG central (h) WB, IP, IF, ELISA h, e, c
Atm (Q-19) Antibody sc-7129 goat IgG N-terminus (h) WB, IP, IF, ELISA m, r, h, c
Atm (R-18) Antibody sc-7128 goat IgG internal (h) WB, IP, IF, ELISA h, e, b, p
Atm (1A1) Antibody sc-73615 mouse IgG1 2581-2860 (h) WB, IP, IF m, r, h
Atm (1B10) Antibody sc-135663 mouse IgG2b N/A WB, IP, ELISA m, r, h
Atm (5C2) Antibody sc-23922 mouse IgG1 980-1512 (h) WB, IP, IF m, r, h
p-Atm (10H11.E12) Antibody sc-47739 mouse IgG1 Ser 1981 (h) WB, IP, IF m, h

Atm specific siRNA, sHRNA Plasmid and shRNA Lentiviral Particles gene silencers are also available.

These include:

siRNAs shRNA Plasmids shRNA Lentiviral Particles
Atm siRNA (h): sc-29761Atm shRNA Plasmid (h): sc-29761-SHAtm shRNA (h)
Lentiviral Particles: sc-29761-V
Atm siRNA (m): sc-29762Atm shRNA Plasmid (m): sc-29762-SHAtm shRNA (m)
Lentiviral Particles: sc-29762-V
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) that 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.