电话:
400-7060-959
传真:
+86 10 56315212-8813
电子邮件:
orders@antibodies-online.cn

DLD 抗体 (Middle Region)

DLD 适用: 人, 小鼠, 大鼠, 犬, 兔, Cow, 马, Saccharomyces cerevisiae, 斑马鱼, 豚鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN2787688
发货至: 中国
  • 抗原 See all DLD 抗体
    DLD (Dihydrolipoamide Dehydrogenase (DLD))
    抗原表位
    • 6
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Middle Region
    适用
    人, 小鼠, 大鼠, 犬, 兔, Cow, 马, Saccharomyces cerevisiae, 斑马鱼, 豚鼠
    宿主
    • 50
    • 5
    克隆类型
    • 48
    • 7
    多克隆
    标记
    • 32
    • 6
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This DLD antibody is un-conjugated
    应用范围
    • 49
    • 22
    • 19
    • 11
    • 9
    • 8
    • 7
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC)
    序列
    AGEMVNEAAL ALEYGASCED IARVCHAHPT LSEAFREANL AASFGKSINF
    预测反应
    Cow: 100%, Dog: 100%, Guinea Pig: 93%, Horse: 100%, Human: 100%, Mouse: 86%, Rabbit: 100%, Rat: 93%, Yeast: 86%, Zebrafish: 93%
    产品特性
    This is a rabbit polyclonal antibody against DLD. It was validated on Western Blot using a cell lysate as a positive control.
    纯化方法
    Affinity Purified
    免疫原
    The immunogen is a synthetic peptide directed towards the middle region of human DLD
    Top Product
    Discover our top product DLD Primary Antibody
  • 应用备注
    Optimal working dilutions should be determined experimentally by the investigator.
    说明

    Antigen size: 509 AA

    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    Lot specific
    缓冲液
    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
    储存液
    Sodium azide
    注意事项
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    注意事项
    Avoid repeated freeze-thaw cycles.
    储存条件
    -20 °C
    储存方法
    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • Ayanniyi, Raji, Adegoke: "Prevalence of asymptomatic sacroiliac joint dysfunction and its association with leg length discrepancies in male students in selected junior secondary schools in Ibadan." in: African journal of medicine and medical sciences, Vol. 37, Issue 1, pp. 37-42, (2008) (PubMed).

  • 抗原
    DLD (Dihydrolipoamide Dehydrogenase (DLD))
    别名
    DLD (DLD 产品)
    别名
    DLDD antibody, DLDH antibody, E3 antibody, GCSL antibody, LAD antibody, PHE3 antibody, AI315664 antibody, AI746344 antibody, wu:fb24b05 antibody, DLD antibody, DDBDRAFT_0183800 antibody, DDBDRAFT_0216232 antibody, DDB_0183800 antibody, DDB_0216232 antibody, sc:d0402 antibody, dihydrolipoamide dehydrogenase antibody, dihydrolipoyl dehydrogenase antibody, deltaD antibody, DLD antibody, Dld antibody, dldh antibody, AT4G16155 antibody, CND05840 antibody, bfmBC antibody, GCSL antibody, LACBIDRAFT_182385 antibody, UREG_06178 antibody, lpd antibody, TAGG_RS02070 antibody, Arnit_2606 antibody, Mesil_1945 antibody, Trad_2118 antibody, Acear_0640 antibody, Fbal_0372 antibody, Ilyop_1890 antibody, Ftrac_1733 antibody, Ocepr_1753 antibody, Intca_2017 antibody, Deima_0504 antibody, dld antibody
    背景
    DLD is the L protein of the mitochondrial glycine cleavage system. The L protein, also named dihydrolipoamide dehydrogenase, is also a component of the pyruvate dehydrogenase complex, the alpha-ketoglutarate dehydrogenase complex, and the branched-chain alpha-keto acide dehydrogenase complex. Mutations in this gene have been identified in patients with E3-deficient maple syrup urine disease and lipoamide dehydrogenase deficiency.This gene encodes the L protein of the mitochondrial glycine cleavage system. The L protein, also named dihydrolipoamide dehydrogenase, is also a component of the pyruvate dehydrogenase complex, the alpha-ketoglutarate dehydrogenase complex, and the branched-chain alpha-keto acide dehydrogenase complex. Mutations in this gene have been identified in patients with E3-deficient maple syrup urine disease and lipoamide dehydrogenase deficiency. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
    Alias Symbols: DLDH, E3, GCSL, LAD, PHE3
    Protein Interaction Partner: HUWE1, FUS, UBC, SUMO1, NEDD8, MDM2, ASB15, PEPD, LDHA, CKB, ASS1, CNDP2, TNFAIP8, DPP3, RPL23, FN1, ATF2, MRPL11, UBAP2, MRPL37, MRPL13, MRPL42, GGH, UQCRC2, UQCRC1, MRPL23, NONO, NDUFB5, NDUFA9, ETFB, DLAT, DBT, AK2, SIRT7, SLC2A4, PSMD4, OGDH, DLD, PDH
    Protein Size: 509
    分子量
    56 kDa
    基因ID
    1738
    NCBI登录号
    NM_000108, NP_000099
    UniProt
    B2R5X0
    途径
    Ribonucleoside Biosynthetic Process, Cell RedoxHomeostasis
You are here:
客服