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细胞表面趋化因子受体4抗体

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  • ¥1900
  • Biorigin
  • 2025年11月22日
  • WB,
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 应用范围

      WB,

    • 抗体英文名

      CXCR4

    • 规格

      100ul

    英文名称 CXCR4
    中文名称 细胞表面趋化因子受体4抗体
    别    名 C-X-C chemokine receptor type 4; CXC-R4; CXCR-4; Stromal cell-derived factor 1 receptor; SDF-1 receptor; Fusin; Leukocyte-derived seven transmembrane domain receptor; LESTR; CD184 antigen; CXCR4_HUMAN.  
    研究领域 肿瘤  免疫学  细胞膜受体  细胞类型标志物  
    抗体来源 Rabbit
    克隆类型 Polyclonal
    交叉反应 Human,  (predicted: Rat, )
    产品应用 WB=1:500-1000 ELISA=1:5000-10000 
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    分 子 量 45kDa
    细胞定位 细胞浆 细胞膜 
    性    状 Liquid
    浓    度 1mg/ml
    免 疫 原 KLH conjugated synthetic peptide derived from human CXCR4 : 
    亚    型 IgG
    纯化方法 affinity purified by Protein A
    储 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
    保存条件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
    PubMed PubMed
    产品介绍 This gene encodes a CXC chemokine receptor specific for stromal cell-derived factor-1. The protein has 7 transmembrane regions and is located on the cell surface. It acts with the CD4 protein to support HIV entry into cells and is also highly expressed in breast cancer cells. Mutations in this gene have been associated with WHIM (warts, hypogammaglobulinemia, infections, and myelokathexis) syndrome. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. Monomer. Can form dimers.

    Function:
    Receptor for the C-X-C chemokine CXCL12/SDF-1 that transduces a signal by increasing intracellular calcium ion levels and enhancing MAPK1/MAPK3 activation. Acts as a receptor for extracellular ubiquitin; leading to enhanced intracellular calcium ions and reduced cellular cAMP levels. Involved in hematopoiesis and in cardiac ventricular septum formation. Also plays an essential role in vascularization of the gastrointestinal tract, probably by regulating vascular branching and/or remodeling processes in endothelial cells. Involved in cerebellar development. In the CNS, could mediate hippocampal-neuron survival. Acts as a coreceptor (CD4 being the primary receptor) for HIV-1 X4 isolates and as a primary receptor for some HIV-2 isolates. Promotes Env-mediated fusion of the virus.

    Subunit:
    Monomer. Can form dimmers.

    Subcellular Location:
    Cell membrane; Multi-pass membrane protein.

    Tissue Specificity:
    Expressed in numerous tissues, such as peripheral blood leukocytes, spleen, thymus, spinal cord, heart, placenta, lung, liver, skeletal muscle, kidney, pancreas, cerebellum, cerebral cortex and medulla (in microglia as well as in astrocytes), brain microvascular, coronary artery and umbilical cord endothelial cells. Isoform 1 is predominant in all tissues tested.

    Post-translational modifications:
    Phosphorylated on agonist stimulation. Rapidly phosphorylated on serine and threonine residues in the C-terminal. Phosphorylation at Ser-324 and Ser-325 leads to recruitment of ITCH, ubiquitination and protein degradation.
    Ubiquitinated by ITCH at the cell membrane on agonist stimulation. The ubiquitin-dependent mechanism, endosomal sorting complex required for transport (ESCRT), then targets CXCR4 for lysosomal degradation. This process is dependent also on prior Ser-/Thr-phosphorylation in the C-terminal of CXCR4. Also binding of ARRB1 to STAM negatively regulates CXCR4 sorting to lysosomes though modulating ubiquitination of SFR5S. Sulfation on Tyr-21 is required for efficient binding of CXCL12/SDF-1alpha and promotes its dimerization.
    O- and N-glycosylated. Asn-11 is the principal site of N-glycosylation. There appears to be very little or no glycosylation on Asn-176. N-glycosylation masks coreceptor function in both X4 and R5 laboratory-adapted and primary HIV-1 strains through inhibiting interaction with their Env glycoproteins. The O-glycosylation chondroitin sulfate attachment does not affect interaction with CXCL12/SDF-1alpha nor its coreceptor activity.

    DISEASE:
    Defects in CXCR4 are a cause of WHIM syndrome (WHIM) [MIM:193670]; also known as warts, hypogammaglobulinemia, infections and myelokathexis. WHIM syndrome is an immunodeficiency disease characterized by neutropenia, hypogammaglobulinemia and extensive human papillomavirus (HPV) infection. Despite the peripheral neutropenia, bone marrow aspirates from affected individuals contain abundant mature myeloid cells, a condition termed myelokathexis.

    Similarity:
    Belongs to the G-protein coupled receptor 1 family.

    SWISS:
    P61073

    Gene ID:
    7852

    Database links:

    Entrez Gene: 7852 Human

    Entrez Gene: 12767 Mouse

    Entrez Gene: 60628 Rat

    Omim: 162643 Human

    SwissProt: P61073 Human

    SwissProt: P70658 Mouse

    SwissProt: O08565 Rat

    Unigene: 593413 Human



    Important Note:
    This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

     

     

     

     

     

     

     

     

     

     

     

     

     

     

     

     

     

     

     

     

     

     

     

     

     

     

     

     

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    图标文献和实验
    相关实验
    • 趋化因子受体

      发现它是HIV感染T细胞的一种协同受体。CXCR5表达于成熟的B细胞表面。SCID鼠由于缺乏成熟的B细胞,脾脏内的CXCR5的水平大大降低。CXCR6主要表达于NKT细胞和活化的工型CD4T细胞和CD8T细胞。 2.CCR趋化因子受体 CCR/基因位于人染色体3p21,成熟分子含355个氨基酸残基,配体为MIP―l。和RAN―TE5;CC只1主要表达于单核细胞、中性粒细胞、T细胞、B细胞和嗜酸粒细胞,以及肺、肝等组织,类风湿关节炎患者的外周血和关节滑液中也检出CCRl。CCR2主要与MIP

    • 趋化因子及其受体

      趋化因子及其受体 趋化因子(chemokine)是一组小分子质量(8―1lkDa)蛋白的集合,是细胞因子家族中惟一作用于G蛋白偶联受体超家族的成员。它们直接参与白细胞特别是吞噬细胞和淋巴细胞的游走和活化,参与炎症反应并在其中起核心作用。趋化因子还具有其他多效性功能,如对肿瘤生长的调节,参与免疫系统、循环系统和神经系统的发育等。 迄今发现的人的趋化因子约有50种。趋化因子的序列相似性较低,但是三维空间结构存在显著的同源性。它们都是单链蛋白,拥有相同的单体

    • 趋化因子受体信号传递

      趋化因子受体信号传递       趋化因子受体与相应配体结合后引发胞内复杂的信号转导级联反应。第一步是受体与其高亲和力配体的结合,引起构象变化导致受体关联的G蛋白异三聚体分解为α和βγ亚基,α和βγ亚基作为第二信使激活随后的一系列效应酶,如磷脂酶C和蛋白激酶。   主要的趋化因子受体、配体及其分布       磷脂酶C可引发磷酸肌醇C信号通路和胞内Ca2+浓度的增加。这个信号转导级联反应不仅可以调节肌动蛋白依赖的细胞

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