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SCARB2 抗体 (C-Term)

This anti-SCARB2 antibody is a 兔 多克隆 antibody detecting SCARB2 in WB. Suitable for 人, 小鼠, 大鼠, Cow, 犬, 马, 兔 和 豚鼠.
产品编号 ABIN2788868
发货至: 中国

Quick Overview for SCARB2 抗体 (C-Term) (ABIN2788868)

抗原

See all SCARB2 抗体
SCARB2 (Scavenger Receptor Class B, Member 2 (SCARB2))

适用

人, 小鼠, 大鼠, Cow, 犬, 马, 兔, 豚鼠

宿主

  • 43
  • 4
  • 2
  • 1

克隆类型

  • 45
  • 5
多克隆

标记

  • 24
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This SCARB2 antibody is un-conjugated

应用范围

  • 38
  • 17
  • 13
  • 13
  • 11
  • 10
  • 6
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB)
  • 抗原表位

    • 15
    • 7
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    C-Term

    序列

    KSMINTTLII TNIPYIIMAL GVFFGLVFTW LACKGQGSMD EGTADERAPL

    预测反应

    Cow: 92%, Dog: 92%, Guinea Pig: 100%, Horse: 92%, Human: 100%, Mouse: 100%, Rabbit: 100%, Rat: 92%

    产品特性

    This is a rabbit polyclonal antibody against SCARB2. It was validated on Western Blot.

    纯化方法

    Affinity Purified

    免疫原

    The immunogen is a synthetic peptide directed towards the C-terminal region of Human SCARB2
  • 应用备注

    Optimal working dilution should be determined by the investigator.

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    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 repeat 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.
  • 抗原

    SCARB2 (Scavenger Receptor Class B, Member 2 (SCARB2))

    别名

    SCARB2

    背景

    The protein encoded by this gene is a type III glycoprotein that is located primarily in limiting membranes of lysosomes and endosomes. Earlier studies in mice and rat suggested that this protein may participate in membrane transportation and the reorganization of endosomal/lysosomal compartment. The protein deficiency in mice was reported to impair cell membrane transport processes and cause pelvic junction obstruction, deafness, and peripheral neuropathy. Further studies in human showed that this protein is a ubiquitously expressed protein and that it is involved in the pathogenesis of HFMD (hand, foot, and mouth disease) caused by enterovirus-71 and possibly by coxsackievirus A16. Mutations in this gene caused an autosomal recessive progressive myoclonic epilepsy-4 (EPM4), also known as action myoclonus-renal failure syndrome (AMRF).
    Alias Symbols: AMRF, CD36L2, EPM4, HLGP85, LGP85, LIMP-2, LIMPII, SR-BII
    Protein Interaction Partner: UBC, ATP4A, TAF15, NONO, HSPD1, DDX1, ATP6V1B1, Ap1g1, AP3S2, AP3S1, THBS1,
    Protein Size: 478

    分子量

    50 kDa

    基因ID

    950

    NCBI登录号

    NM_005506, NP_005497

    UniProt

    Q14108
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