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BBS2 抗体 (Middle Region)

BBS2 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN929334
发货至: 中国
  • 抗原 See all BBS2 抗体
    BBS2 (Bardet-Biedl Syndrome 2 (BBS2))
    抗原表位
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Middle Region
    适用
    • 10
    • 6
    • 4
    • 4
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    宿主
    • 8
    • 3
    克隆类型
    • 10
    • 1
    多克隆
    标记
    • 11
    This BBS2 antibody is un-conjugated
    应用范围
    • 11
    • 4
    • 3
    • 2
    • 1
    Western Blotting (WB)
    纯化方法
    Purified
    免疫原
    BBS2 antibody was raised in rabbit using the middle region of BBS2 as the immunogen
    Top Product
    Discover our top product BBS2 Primary Antibody
  • 应用备注
    WB: 0.2-1 µg/mL
    Optimal conditions should be determined by the investigator.
    说明

    BBS2 Blocking Peptide, catalog no. 33R-7948, is also available for use as a blocking control in assays to test for specificity of this BBS2 antibody

    限制
    仅限研究用
  • 状态
    Lyophilized
    浓度
    Lot specific
    缓冲液
    Lyophilized powder. Add 50 µL of distilled water. Final antibody concentration is 1 mg/mL in PBS buffer.
    注意事项
    Avoid repeated freeze/thaw cycles.
    储存条件
    4 °C/-20 °C
    储存方法
    Store at 4 °C, following reconstitution, aliquot and store at -20 °C.
  • 抗原
    BBS2 (Bardet-Biedl Syndrome 2 (BBS2))
    别名
    BBS2 (BBS2 产品)
    别名
    fb80a05 antibody, wu:fb80a05 antibody, DKFZp468B105 antibody, DKFZp469L0919 antibody, BBS antibody, 2410125H22Rik antibody, AI447581 antibody, Bardet-Biedl syndrome 2 antibody, bardet-biedl syndrome 2 antibody, Bardet-Biedl syndrome 2 (human) antibody, bbs2 antibody, BBS2 antibody, Bbs2 antibody
    背景
    This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation and mental retardation. The proteins encoded by BBS gene family members are structurally diverse and the similar phenotypes exhibited by mutations in BBS gene family members is likely due to their shared roles in cilia formation and function. Many BBS proteins localize to the basal bodies, ciliary axonemes, and pericentriolar regions of cells. BBS proteins may also be involved in intracellular trafficking via microtubule-related transport. The protein encoded by this gene forms a multiprotein BBSome complex with six other BBS proteins. Synonyms: Polyclonal BBS2 antibody, Anti-BBS2 antibody, Bardet-Biedl syndrome 2 antibody, BBS antibody, MGC20703 antibody.
    途径
    Hedgehog Signaling
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