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TPM3 抗体 (Middle Region)

TPM3 适用: 人, 小鼠, 大鼠, 兔, Cow, 斑马鱼, 犬, 豚鼠, 马 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN2776646
发货至: 中国
  • 抗原 See all TPM3 抗体
    TPM3 (Tropomyosin 3 (TPM3))
    抗原表位
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Middle Region
    适用
    • 27
    • 16
    • 12
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    人, 小鼠, 大鼠, 兔, Cow, 斑马鱼, 犬, 豚鼠, 马
    宿主
    • 25
    • 5
    克隆类型
    • 26
    • 4
    多克隆
    标记
    • 19
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This TPM3 antibody is un-conjugated
    应用范围
    • 18
    • 10
    • 10
    • 5
    • 3
    • 3
    • 3
    • 1
    • 1
    Western Blotting (WB)
    序列
    TEERAELAES RCREMDEQIR LMDQNLKCLS AAEEKYSQKE DKYEEEIKIL
    预测反应
    Cow: 100%, Dog: 100%, Guinea Pig: 100%, Horse: 100%, Human: 100%, Mouse: 100%, Rabbit: 100%, Rat: 100%, Zebrafish: 100%
    产品特性
    This is a rabbit polyclonal antibody against TPM3. 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 TPM3
    Top Product
    Discover our top product TPM3 Primary Antibody
  • 应用备注
    Optimal working dilutions should be determined experimentally by the investigator.
    说明

    Antigen size: 285 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.
  • Ramsey, Clarke, Roberts, Sullivan, Johnson, Liu: "An economic evaluation of atorvastatin for primary prevention of cardiovascular events in type 2 diabetes." in: PharmacoEconomics, Vol. 26, Issue 4, pp. 329-39, (2008) (PubMed).

  • 抗原
    TPM3 (Tropomyosin 3 (TPM3))
    别名
    TPM3 (TPM3 产品)
    别名
    CAPM1 antibody, CFTD antibody, NEM1 antibody, OK/SW-cl.5 antibody, TM-5 antibody, TM3 antibody, TM30 antibody, TM30nm antibody, TM5 antibody, TPMsk3 antibody, TRK antibody, hscp30 antibody, cb674 antibody, fa17b11 antibody, fb83b01 antibody, fk41e01 antibody, hm:zeh0298 antibody, wu:fa17b11 antibody, wu:fb83b01 antibody, wu:fk41e01 antibody, zeh0298 antibody, zgc:77592 antibody, TPM3 antibody, Tm5NM antibody, Tpm-5 antibody, Tpm5 antibody, Trop-5 antibody, gamma-TM antibody, hTM30nm antibody, hTMnm antibody, tm3 antibody, tpm3 antibody, tpm3.L antibody, tropomyosin 3 antibody, tropomyosin 3, gamma antibody, tropomyosin 3 S homeolog antibody, TPM3 antibody, tpm3 antibody, Tpm3 antibody, tpm3.S antibody
    背景
    TPM3 is a member of the tropomyosin family of actin-binding proteins involved in the contractile system of striated and smooth muscles and the cytoskeleton of non-muscle cells. Tropomyosins are dimers of coiled-coil proteins that polymerize end-to-end along the major groove in most actin filaments. They provide stability to the filaments and regulate access of other actin-binding proteins. In muscle cells, they regulate muscle contraction by controlling the binding of myosin heads to the actin filament. Mutations in this gene result in autosomal dominant nemaline myopathy, and oncogenes formed by chromosomal translocations involving this locus are associated with cancer.This gene encodes a member of the tropomyosin family of actin-binding proteins involved in the contractile system of striated and smooth muscles and the cytoskeleton of non-muscle cells. Tropomyosins are dimers of coiled-coil proteins that polymerize end-to-end along the major groove in most actin filaments. They provide stability to the filaments and regulate access of other actin-binding proteins. In muscle cells, they regulate muscle contraction by controlling the binding of myosin heads to the actin filament. Mutations in this gene result in autosomal dominant nemaline myopathy, and oncogenes formed by chromosomal translocations involving this locus are associated with cancer. Multiple transcript variants encoding different isoforms have been found for this gene.
    Alias Symbols: FLJ41118, MGC14582, MGC3261, MGC72094, NEM1, OK/SW-cl.5, TM-5, TM3, TM30, TM30nm, TPMsk3, TRK, hscp30, TM5, CFTD, hTM5
    Protein Interaction Partner: TLK1, MAD1L1, TRIP6, TPM3, TP53, TNNT1, VPS52, TRIM27, PBX3, MAGEA11, KIFC3, KCNE1, IFIT3, HSF2, LURAP1, WASH3P, HDDC3, FAM9C, LCA5L, C1orf216, IKBIP, SYCE1, CCDC114, CCDC102B, KXD1, CCDC146, THAP1, CCHCR1, TFPT, BLOC1S6, OIP5, UBC, MDM2, RNF2, MAGED2, MG
    Protein Size: 285
    分子量
    33 kDa
    基因ID
    7170
    NCBI登录号
    NM_153649, NP_705935
    UniProt
    P06753
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