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SLC29A3 抗体 (N-Term)

SLC29A3 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB32652 unconjugated
产品编号 ABIN656792
发货至: 中国
  • 抗原 See all SLC29A3 抗体
    SLC29A3 (Solute Carrier Family 29 Member 3 (SLC29A3))
    抗原表位
    • 7
    • 7
    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 21-50, N-Term
    适用
    • 20
    • 6
    • 5
    • 3
    • 3
    宿主
    • 21
    克隆类型
    • 21
    多克隆
    标记
    • 9
    • 3
    • 3
    • 2
    • 2
    • 2
    This SLC29A3 antibody is un-conjugated
    应用范围
    • 20
    • 16
    • 15
    • 3
    • 3
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    纯化方法
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    免疫原
    This SLC29A3 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 21-50 amino acids from the N-terminal region of human SLC29A3.
    克隆位点
    RB32652
    亚型
    Ig Fraction
    Top Product
    Discover our top product SLC29A3 Primary Antibody
  • 应用备注
    WB: 1:1000. IHC-P: 1:10~50
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
    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.
    储存条件
    4 °C,-20 °C
    储存方法
    SLC29A3 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.
    有效期
    6 months
  • 抗原
    SLC29A3 (Solute Carrier Family 29 Member 3 (SLC29A3))
    别名
    SLC29A3 (SLC29A3 产品)
    别名
    ENT3 antibody, HCLAP antibody, HJCD antibody, PHID antibody, Ent3 antibody, 4933435C21Rik antibody, AW987637 antibody, solute carrier family 29 member 3 antibody, solute carrier family 29 (nucleoside transporters), member 3 antibody, SLC29A3 antibody, Slc29a3 antibody
    背景
    This gene encodes a nucleoside transporter. The encoded protein plays a role in cellular uptake of nucleosides, nucleobases, and their related analogs. Mutations in this gene have been associated with H syndrome, which is characterized by cutaneous hyperpigmentation and hypertrichosis, hepatosplenomegaly, heart anomalies, and hypogonadism. A related disorder, PHID (pigmented hypertrichosis with insulin-dependent diabetes mellitus), has also been associated with mutations at this locus. Alternatively spliced transcript variants have been described.
    分子量
    51815
    基因ID
    55315
    NCBI登录号
    NP_001167569, NP_060814
    UniProt
    Q9BZD2
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