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CD45 Monoclonal Antibody(12A9)
商品货号: PLA005618
适 应 性:
WB IHC IF
¥600元
规格:
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MSDS
说明书
商品描述
  • 基因名称: PTPRC
  • 蛋白名称: Receptor-type tyrosine-protein phosphatase C
  • Human_gene_id: 5788
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=5788
  • Human_swiss_prot_no: P08575
  • Human_swiss_link: http://www.uniprot.org/uniprotkb/P08575/entry
  • Mouse_swiss_prot_no: P06800
  • Mouse_swiss_link: http://www.uniprot.org/uniprot/P06800
  • Rat_gene_id: 24699
  • Rat_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=24699
  • Rat_swiss_prot_no: P04157
  • Rat_swiss_link: http://www.uniprot.org/uniprot/P04157
  • 特异性: The antibody detects endogenous CD45 proteins.
  • 组成: PBS, pH 7.4, containing 0.5%BSA, 0.02% sodium azide as Preservative and 50% Glycerol.
  • 来源: Monoclonal, Mouse
  • 稀释: IF 1:50-200 WB 1:2000 IHC 1:50-300
  • 纯化工艺: The antibody was affinity-purified from mouse ascites by affinity-chromatography using specific immunogen.
  • 储存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 说明书: 1
  • Msds: MSDS_Antibody.pdf
  • 其他名称: PTPRC; CD45; Receptor-type tyrosine-protein phosphatase C; Leukocyte common antigen; L-CA; T200; CD45
  • 实测条带: 147kD
  • 信号通路: Cell adhesion molecules (CAMs);T_Cell_Receptor;Fc gamma R-mediated phagocytosis;Primary immunodeficiency;
  • 功能: alternative products:At least 8 isoforms are produced,catalytic activity:Protein tyrosine phosphate + H(2)O = protein tyrosine + phosphate.,disease:Defects in PTPRC are a cause of severe combined immunodeficiency autosomal recessive T-cell-negative/B-cell-positive/NK-cell-positive (T(-)B(+)NK(+)SCID) [MIM:608971]. SCID refers to a genetically and clinically heterogeneous group of rare congenital disorders characterized by impairment of both humoral and cell-mediated immunity, leukopenia, and low or absent antibody levels. Patients with SCID present in infancy with recurrent, persistent infections by opportunistic organisms. The common characteristic of all types of SCID is absence of T-cell-mediated cellular immunity due to a defect in T-cell development.,disease:Genetic variations in PTPRC are involved in multiple sclerosis susceptibility (MS) [MIM:126200]. MS is a neurodegenerative disorder characterized by the gradual accumulation of focal plaques of demyelination particularly in the periventricular areas of the brain. Peripheral nerves are not affected. Onset usually in third or fourth decade with intermittent progression over an extended period. The cause is still uncertain.,domain:The first PTPase domain interacts with SKAP1.,function:Required for T-cell activation through the antigen receptor. The first PTPase domain has enzymatic activity, while the second one seems to affect the substrate specificity of the first one. Upon T-cell activation, recruits an dephosphorylates SKAP1 and FYN.,online information:CD45 entry,online information:PTPRC mutation db,PTM:Heavily N- and O-glycosylated.,similarity:Belongs to the protein-tyrosine phosphatase family. Receptor class 1/6 subfamily.,similarity:Contains 2 fibronectin type-III domains.,similarity:Contains 2 tyrosine-protein phosphatase domains.,subunit:Binds GANAB and PRKCSH (By similarity). Interacts with SKAP1.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Cell membrane ; Single-pass type I membrane protein . Membrane raft . Colocalized with DPP4 in membrane rafts. .
  • 组织表达: Isoform 1: Detected in thymocytes. Isoform 2: Detected in thymocytes. Isoform 3: Detected in thymocytes. Isoform 4: Not detected in thymocytes. Isoform 5: Detected in thymocytes. Isoform 6: Not detected in thymocytes. Isoform 7: Detected in thymocytes. Isoform 8: Not detected in thymocytes.
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  • 科研货号: PLA005618
CD45 Monoclonal Antibody(12A9)
Catalog No PLA005618
Product information
  • 基因名称: PTPRC
  • 蛋白名称: Receptor-type tyrosine-protein phosphatase C
  • Human_gene_id: 5788
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=5788
  • Human_swiss_prot_no: P08575
  • Human_swiss_link: http://www.uniprot.org/uniprotkb/P08575/entry
  • Mouse_swiss_prot_no: P06800
  • Mouse_swiss_link: http://www.uniprot.org/uniprot/P06800
  • Rat_gene_id: 24699
  • Rat_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=24699
  • Rat_swiss_prot_no: P04157
  • Rat_swiss_link: http://www.uniprot.org/uniprot/P04157
  • 特异性: The antibody detects endogenous CD45 proteins.
  • 组成: PBS, pH 7.4, containing 0.5%BSA, 0.02% sodium azide as Preservative and 50% Glycerol.
  • 来源: Monoclonal, Mouse
  • 稀释: IF 1:50-200 WB 1:2000 IHC 1:50-300
  • 纯化工艺: The antibody was affinity-purified from mouse ascites by affinity-chromatography using specific immunogen.
  • 储存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 说明书: 1
  • Msds: MSDS_Antibody.pdf
  • 其他名称: PTPRC; CD45; Receptor-type tyrosine-protein phosphatase C; Leukocyte common antigen; L-CA; T200; CD45
  • 实测条带: 147kD
  • 信号通路: Cell adhesion molecules (CAMs);T_Cell_Receptor;Fc gamma R-mediated phagocytosis;Primary immunodeficiency;
  • 功能: alternative products:At least 8 isoforms are produced,catalytic activity:Protein tyrosine phosphate + H(2)O = protein tyrosine + phosphate.,disease:Defects in PTPRC are a cause of severe combined immunodeficiency autosomal recessive T-cell-negative/B-cell-positive/NK-cell-positive (T(-)B(+)NK(+)SCID) [MIM:608971]. SCID refers to a genetically and clinically heterogeneous group of rare congenital disorders characterized by impairment of both humoral and cell-mediated immunity, leukopenia, and low or absent antibody levels. Patients with SCID present in infancy with recurrent, persistent infections by opportunistic organisms. The common characteristic of all types of SCID is absence of T-cell-mediated cellular immunity due to a defect in T-cell development.,disease:Genetic variations in PTPRC are involved in multiple sclerosis susceptibility (MS) [MIM:126200]. MS is a neurodegenerative disorder characterized by the gradual accumulation of focal plaques of demyelination particularly in the periventricular areas of the brain. Peripheral nerves are not affected. Onset usually in third or fourth decade with intermittent progression over an extended period. The cause is still uncertain.,domain:The first PTPase domain interacts with SKAP1.,function:Required for T-cell activation through the antigen receptor. The first PTPase domain has enzymatic activity, while the second one seems to affect the substrate specificity of the first one. Upon T-cell activation, recruits an dephosphorylates SKAP1 and FYN.,online information:CD45 entry,online information:PTPRC mutation db,PTM:Heavily N- and O-glycosylated.,similarity:Belongs to the protein-tyrosine phosphatase family. Receptor class 1/6 subfamily.,similarity:Contains 2 fibronectin type-III domains.,similarity:Contains 2 tyrosine-protein phosphatase domains.,subunit:Binds GANAB and PRKCSH (By similarity). Interacts with SKAP1.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Cell membrane ; Single-pass type I membrane protein . Membrane raft . Colocalized with DPP4 in membrane rafts. .
  • 组织表达: Isoform 1: Detected in thymocytes. Isoform 2: Detected in thymocytes. Isoform 3: Detected in thymocytes. Isoform 4: Not detected in thymocytes. Isoform 5: Detected in thymocytes. Isoform 6: Not detected in thymocytes. Isoform 7: Detected in thymocytes. Isoform 8: Not detected in thymocytes.
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  • 科研货号: PLA005618
  • Hunan UPT Biotechnology Co.,Ltd
    Website:www.uptbio.com Servive hotline :4006916686
    E-mail:service@uptbio.com
    Address:
    Room 402, Building 13, Xinggong International Industrial Park, 100 Guyuan Road, Yuelu District, Changsha City, Hunan Province, China.
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