merck millipore,默克密理博,04-200,Anti-ATM Antibody, clone Y170, rabbit monoclonal

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merck millipore,默克密理博,04-200,Anti-ATM Antibody, clone Y170, rabbit monoclonal
产品名称：Anti-ATM Antibody, clone Y170, rabbit monoclonal
产品型号：04-200
Please note that this product will not be available for sale after March 15, 2015. Please select one of the other antibodies against this target. This Anti-ATM Antibody, clone Y170, Rabbit is valida More>>

merck millipore,默克密理博,04-200,Anti-ATM Antibody, clone Y170, rabbit monoclonal

产品介绍

merck millipore,默克密理博,04-200,Anti-ATM Antibody, clone Y170, rabbit monoclonal

重要规格表

品种反应性	主要应用	宿主	格式	抗体类型
H	WB, ICC, IHC	Rb	Culture Supernatant	Monoclonal Antibody

描述
产品目录编号	04-200
品牌系列	Upstate
商名	Upstate
描述	Anti-ATM Antibody, clone Y170, rabbit monoclonal
Alternate Names	serine-protein kinase ATM A-T, mutated AT mutated TEL1, telomere maintenance 1, homolog ataxia telangiectasia mutated ataxia telangiectasia mutated (includes complementation groups A, C and D) ataxia telangiectasia mutated protein human phosphatidylinositol 3-kinase homolog ataxia telangiectasia mutated (includes complementation groups A C and D) ataxia telangiectasia mutated protein human phosphatidylinositol 3-kinase homolog
背景信息	ATM (Ataxia Telangiectasia Mutated kinase) and ATR (Ataxia Telangiectasia and Rad3-related kinase) are related kinases that regulate cell cycle checkpoints and DNA repair. ATM is activated in response to DNA damage and serves to arrest further cell division before the damage can be repaired. Mutation in the ATM gene results in the autosomal recessive disease ataxia telangiectasia (AT). The identified substrates for ATM are p53, p95/NBS1, MDM2, Chk2, BRCA1, CtIP, 4E-BP1 and Chk1. ATM activates p53, increasing p21/Cip1/Waf1 levels, thus blocking activation of Cdk2. That results in Rb hypophosphorylation and blockage of the G1/S transition. Separately, ATM also phosphorylates and activates Chk1, which phosphorylates Cdc25C. This inactivates Cdc25C and prevents it from dephosphorylating the inhibitory phosphotyrosine residue on cdc2/Cdk1, thus preventing the G2/M transition. The complex phenotype of cells derived from patients with AT suggests that ATM has additional cellular substrates. In unirradiated cells, ATM is present as an inactive homodimer or multimer. Double-stranded breaks in DNA caused by ionizing radiation cause rapid ATM kinase activation through dissociation of this complex and ATM autophosphorylation at Ser1981.

产品信息
格式	Culture Supernatant
控制	HEK293 cell lysate.
演示	Unpurified rabbit monoclonal IgG in buffer containing 50 mM Tris-Glycine (pH 7.4), 0.15 M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% BSA.

应用
应用	Please note that this product will not be available for sale after March 15, 2015. Please select one of the other antibodies against this target. This Anti-ATM Antibody, clone Y170, Rabbit is validated for use in IC, IF, IH, IH(P), IP, WB for the detection of ATM.
主要应用	Western Blotting Immunocytochemistry Immunohistochemistry
应用说明	Immunocytochemistry: A 1:100-250 dilution of a previous lot of this antibody was used on immunocytochemistry. Immunohistochemistry: A 1:250 dilution of a previous lot of this antibody was used on immunohistochemistry. Immunoprecipitation: A 1:50 dilution of a previous lot of this antibody was used on immunoprecipitation.

生物信息
免疫原品种	Synthetic peptide corresponding to the FAT domain encompassing the area of Ser1981 of human ATM.
表位	area encompassing the autophosphorylation site at Ser1981 in the FAT Domain
克隆	Y170
宿主	Rabbit
特异性	This antibody recognizes ATM irrespective of phosphorylation on Ser1981.
同种型	IgG
品种反应性	Human
Species Reactivity Note	Proven to react with human. Not expected to react with mouse or rat.
抗体类型	Monoclonal Antibody
Entrez基因编号	NM_000051.3
Entrez基因汇总	The protein encoded by this gene belongs to the PI3/PI4-kinase family. This protein is an important cell cycle checkpoint kinase that phosphorylates; thus, it functions as a regulator of a wide variety of downstream proteins, including tumor suppressor proteins p53 and BRCA1, checkpoint kinase CHK2, checkpoint proteins RAD17 and RAD9, and DNA repair protein NBS1. This protein and the closely related kinase ATR are thought to be master controllers of cell cycle checkpoint signaling pathways that are required for cell response to DNA damage and for genome stability. Mutations in this gene are associated with ataxia telangiectasia, an autosomal recessive disorder. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq].
基因符号	TELO1 AT1 ATA ATC ATD ATDC ATE DKFZp781A0353 EC 2.7.11.1 MGC74674 TEL1
非反应性品种	Rat Mouse
纯化方法	Unpurified
UniProt编号	Q13315
UniProt汇总	FUNCTION:Serine/threonine protein kinase which activates checkpoint signaling upon double strand breaks (DSBs), apoptosis and genotoxic stresses such as ionizing ultraviolet A light (UVA), thereby acting as a DNA damage sensor. Recognizes the substrate consensus sequence [ST]-Q. Phosphorylates 'Ser-139' of histone variant H2AX/H2AFX at double strand breaks (DSBs), thereby regulating DNA damage response mechanism. Also involved in signal transduction and cell cycle control. May function as a tumor suppressor. Necessary for activation of ABL1 and SAPK. Phosphorylates p53/TP53, FANCD2, NFKBIA, BRCA1, CTIP, nibrin (NBN), TERF1, RAD9 and DCLRE1C. May play a role in vesicle and/or protein transport. Could play a role in T-cell development, gonad and neurological function. Catalytic activity ATP + a protein = ADP + a phosphoprotein. Enzyme regulation Inhibited by wortmannin. Ref.14 STRUCTURE: Exists in monomeric and tetrameric state. Binds DNA ends, p53/TP53, ABL1, BRCA1, NBN/nibrin and TERF1. Part of the BRCA1-associated genome surveillance complex (BASC), which contains BRCA1, MSH2, MSH6, MLH1, ATM, BLM, PMS2 and the RAD50-MRE11-NBN protein complex. This association could be a dynamic process changing throughout the cell cycle and within subnuclear domains. DNA damage promotes association with RAD17. Interacts with EEF1E1. This interaction, which takes place independently of TP53, is induced by DNA damage that may occur during genotoxic stress or cell growth. Interacts with DCLRE1C. Interacts with MYST1. Interacts with HTATIP. Interacts with OBFC2B. Interacts with ATMIN. Ref.13 Ref.15 Ref.16 Ref.27 Ref.30 Ref.32 Ref.33 Ref.34 Ref.35 Ref.38 SUBCELLULAR LOCATION: Nucleus. Cytoplasmic vesicle. Note= Primarily nuclear. Found also in endocytic vesicles in association with beta-adaptin. Ref.10 Ref.11 SPECIFICITY: Found in pancreas, kidney, skeletal muscle, liver, lung, placenta, brain, heart, spleen, thymus, testis, ovary, small intestine, colon and leukocytes. INDUCTION:By ionizing radiation. DOMAIN: The FATC domain is required for interaction with HTATIP. PTM: Phosphorylated by ARK5. Autophosphorylated on Ser-1981 upon DNA damage. Ref.34 Ref.9 Ref.17 Ref.18 Ref.20 Ref.22 Ref.23 Ref.24 Ref.25 Ref.26 Ref.28 Ref.29 Ref.31 Ref.36 Ref.37 Acetylated by HTATIP upon DNA damage; which is required for autophosphorylation and subsequent activation. DISEASE: Defects in ATM are the cause of ataxia telangiectasia (AT) [MIM:208900]; also known as Louis-Bar syndrome, which includes four complementation groups: A, C, D and E. This rare recessive disorder is characterized by progressive cerebellar ataxia, dilation of the blood vessels in the conjunctiva and eyeballs, immunodeficiency, growth retardation and sexual immaturity. AT patients have a strong predisposition to cancer; about 30% of patients develop tumors, particularly lymphomas and leukemias. Cells from affected individuals are highly sensitive to damage by ionizing radiation and resistant to inhibition of DNA synthesis following irradiation. Ref.34 Ref.35 Ref.11 Ref.31 Ref.36 Ref.37 Ref.4 Ref.7 Ref.21 Ref.39 Ref.40 Ref.41 Ref.42 Ref.43 Ref.44 Ref.47 Ref.48 Ref.49 Ref.50 Ref.52 Ref.53 Ref.54 Ref.55 Ref.56 Ref.61 Ref.63 Ref.64 Ref.68 Ref.69 Defects in ATM contribute to T-cell acute lymphoblastic leukemia (TALL) and T-prolymphocytic leukemia (TPLL). TPLL is characterized by a high white blood cell count, with a predominance of prolymphocytes, marked splenomegaly, lymphadenopathy, skin lesions and serous effusion. The clinical course is highly aggressive, with poor response to chemotherapy and short survival time. TPLL occurs both in adults as a sporadic disease and in younger AT patients. Defects in ATM contribute to B-cell non-Hodgkin lymphomas (BNHL), including mantle cell lymphoma (MCL). Ref.45 Defects in ATM contribute to B-cell chronic lymphocytic leukemia (BCLL). BCLL is the commonest form of leukemia in the elderly. It is characterized by the accumulation of mature CD5+ B lymphocytes, lymphadenopathy, immunodeficiency and bone marrow failure. Ref.59 Ref.60 Ref.65 SIMILARITY: Belongs to the PI3/PI4-kinase family. ATM subfamily. Contains 1 FAT domain. Contains 1 FATC domain. Contains 1 PI3K/PI4K domain.

产品使用声明
质量保证	Routinely evaluated by Western Blot on HEK293 cell lysate. Western Blot Analysis: A 1:2,500-1:5,000 dilution of this lot was used to detect ATM in HEK293 cell lysate.
使用声明	Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

储存和货运信息
存储条件	Stable for 1 year at -20ºC from date of receipt. Handling Recommendations: Upon receipt, and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance. Note: Variability in freezer temperatures below -20°C may cause glycerol containing solutions to become frozen during storage.

储存和货运信息

存储条件

Stable for 1 year at -20ºC from date of receipt.
Handling Recommendations: Upon receipt, and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance. Note: Variability in freezer temperatures below -20°C may cause glycerol containing solutions to become frozen during storage.