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SLC25A20 抗体 (C-Term)

SLC25A20 适用: 小鼠, 人, 大鼠, 绵羊, Cow, 马, 犬, 兔, 豚鼠, 斑马鱼 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN2781540
发货至: 中国
  • 抗原 See all SLC25A20 抗体
    SLC25A20 (Solute Carrier Family 25 (Carnitine/acylcarnitine Translocase), Member 20 (SLC25A20))
    抗原表位
    • 15
    • 7
    • 7
    • 6
    • 5
    • 1
    • 1
    • 1
    C-Term
    适用
    • 33
    • 18
    • 6
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    小鼠, 人, 大鼠, 绵羊, Cow, 马, 犬, 兔, 豚鼠, 斑马鱼
    宿主
    • 45
    • 3
    克隆类型
    • 45
    • 3
    多克隆
    标记
    • 17
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    This SLC25A20 antibody is un-conjugated
    应用范围
    • 38
    • 18
    • 13
    • 13
    • 6
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    Western Blotting (WB)
    序列
    GGIAGIFNWA VAIPPDVLKS RFQTAPPGKY PNGFRDVLRE LIRDEGVTSL
    预测反应
    Cow: 100%, Dog: 100%, Guinea Pig: 100%, Horse: 100%, Human: 100%, Mouse: 100%, Rabbit: 100%, Rat: 100%, Sheep: 100%, Zebrafish: 93%
    产品特性
    This is a rabbit polyclonal antibody against SLC25A20. 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 C terminal region of human SLC25A20
    Top Product
    Discover our top product SLC25A20 Primary Antibody
  • 应用备注
    Optimal working dilutions should be determined experimentally by the investigator.
    说明

    Antigen size: 301 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.
  • Pierre, Macdonald, Gray, Hendriksz, Preece, Chakrapani: "Prospective treatment in carnitine-acylcarnitine translocase deficiency." in: Journal of inherited metabolic disease, Vol. 30, Issue 5, pp. 815, (2007) (PubMed).

  • 抗原
    SLC25A20 (Solute Carrier Family 25 (Carnitine/acylcarnitine Translocase), Member 20 (SLC25A20))
    别名
    SLC25A20 (SLC25A20 产品)
    别名
    5848 antibody, BG:DS02740.15 antibody, CACT antibody, CG5848 antibody, Cact antibody, Dmel\\CG5848 antibody, cac antibody, dip6 antibody, fs(2)ltoRN48 antibody, n(2)k17003 antibody, cact antibody, dif-1 antibody, SLC25A20 antibody, DKFZp468F1219 antibody, zgc:77760 antibody, PRKAR2A antibody, CAC antibody, 1110007P09Rik antibody, C78826 antibody, mCAC antibody, cactus antibody, solute carrier family 25 (carnitine/acylcarnitine translocase), member 20 antibody, solute carrier family 25 member 20 antibody, solute carrier family 25 (carnitine/acylcarnitine translocase), member 20 L homeolog antibody, solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20 antibody, cact antibody, slc25a20 antibody, SLC25A20 antibody, Slc25a20 antibody, slc25a20.L antibody
    背景
    SLC25A20 is one of several closely related mitochondrial-membrane carrier proteins that shuttle substrates between cytosol and the intramitochondrial matrix space.It mediates the transport of acylcarnitines into mitochondrial matrix for their oxidation by the mitochondrial fatty acid-oxidation pathway. Mutations in this gene are associated with carnitine-acylcarnitine translocase deficiency, which can cause a variety of pathological conditions such as hypoglycemia, cardiac arrest, hepatomegaly, hepatic dysfunction and muscle weakness, and is usually lethal in new born and infants.This gene product is one of several closely related mitochondrial-membrane carrier proteins that shuttle substrates between cytosol and the intramitochondrial matrix space. This protein mediates the transport of acylcarnitines into mitochondrial matrix for their oxidation by the mitochondrial fatty acid-oxidation pathway. Mutations in this gene are associated with carnitine-acylcarnitine translocase deficiency, which can cause a variety of pathological conditions such as hypoglycemia, cardiac arrest, hepatomegaly, hepatic dysfunction and muscle weakness, and is usually lethal in new born and infants. 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: CAC, CACT
    Protein Interaction Partner: KDM1A, ESR1, UBC, HN1L,
    Protein Size: 301
    分子量
    33 kDa
    基因ID
    788
    NCBI登录号
    NM_000387, NP_000378
    UniProt
    P97521
    途径
    TCR Signaling, Production of Molecular Mediator of Immune Response, Maintenance of Protein Location, Toll-Like Receptors Cascades
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