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RDH5 抗体 (Middle Region)

RDH5 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN5516226
发货至: 中国
  • 抗原 See all RDH5 抗体
    RDH5 (Retinol Dehydrogenase 5 (11-Cis/9-Cis) (RDH5))
    抗原表位
    • 2
    • 1
    • 1
    Middle Region
    适用
    • 8
    • 3
    • 2
    宿主
    • 6
    • 1
    • 1
    克隆类型
    • 8
    多克隆
    标记
    • 8
    This RDH5 antibody is un-conjugated
    应用范围
    • 4
    • 4
    • 4
    • 3
    • 1
    • 1
    Western Blotting (WB)
    序列
    RGFRVLASCL TPSGAEDLQR VASSRLHTTL LDITDPQSVQ QAAKWVEMHV
    纯化方法
    Affinity purified
    免疫原
    The immunogen is a synthetic peptide directed towards the middle terminal region of human RDH5
    Top Product
    Discover our top product RDH5 Primary Antibody
  • 应用备注
    Optimal working dilution should be determined by the investigator.
    限制
    仅限研究用
  • 状态
    Liquid
    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.
    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.
  • 抗原
    RDH5 (Retinol Dehydrogenase 5 (11-Cis/9-Cis) (RDH5))
    别名
    RDH5 (RDH5 产品)
    别名
    9cRDH antibody, HSD17B9 antibody, RDH1 antibody, SDR9C5 antibody, RDHB antibody, MGC84134 antibody, RDH5 antibody, rdh1 antibody, hsd17b9 antibody, im:6901729 antibody, si:dkey-102c8.5 antibody, 9-cis antibody, AI987873 antibody, RDH4 antibody, cRDH antibody, retinol dehydrogenase 5 antibody, retinol dehydrogenase 1 antibody, retinol dehydrogenase 5 L homeolog antibody, retinol dehydrogenase 5 (11-cis/9-cis) antibody, RDH5 antibody, rdh1 antibody, rdh5.L antibody, rdh5 antibody, Rdh5 antibody
    背景
    This gene encodes an enzyme belonging to the short-chain dehydrogenases/reductases (SDR) family. This retinol dehydrogenase functions to catalyze the final step in the biosynthesis of 11-cis retinaldehyde, which is the universal chromophore of visual pigments. Mutations in this gene cause autosomal recessive fundus albipunctatus, a rare form of night blindness that is characterized by a delay in the regeneration of cone and rod photopigments. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the neighboring upstream BLOC1S1 (biogenesis of lysosomal organelles complex-1, subunit 1) gene.

    Alias Symbols: RDH1, 9cRDH, SDR9C5, HSD17B9

    Protein Size: 318
    基因ID
    5959
    NCBI登录号
    NM_001199771, NP_001186700
    UniProt
    Q92781
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