BAALC Antibody Blocking Peptide(bs-9849P)-500ug

BAALC Antibody Blocking Peptid

e(bs-9849P)-500ug
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  • ¥880
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  • bs-9849P
  • 2025年10月16日
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      500ug

    产品编号bs-9849P
    英文名称BAALC Antibody Blocking Peptide
    中文名称脑和急性白血病胞浆蛋白封闭多肽
    英文别名BAALC; BAALC_HUMAN; Brain and acute leukemia cytoplasmic; Brain and acute leukemia cytoplasmic protein; brain and acute leukemia, cytoplasmic; FLJ12015.
    纯化方法HPLC
    亚基Interacts with CAMK2A (By similarity).
    亚细胞定位Cytoplasm. Membrane. Postsynaptic lipid rafts.
    组织特异性Expressed by neural and hematopoietic cells. Expression is found both in normal early progenitor cells and in the most immature type of blasts in acute leukemia but not in mature hematopoietic cells. Isoform 2 and isoform 6 are expressed in the brain. Isoform 2 shows a low expression in neuroectoderm-derived tissues such as adrenal gland and no expression in bone marrow, peripheral blood lymphocytes or lymph nodes, or in tumors or cancer cell lines of nonneural tissue origin.
    翻译后修饰Palmitoylation and myristoylation target the protein to the lipid rafts (By similarity).
    功能May play a synaptic role at the postsynaptic lipid rafts by interacting with CAMK2A (By similarity).
    保存条件Shipped at 4℃. Stored at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    注意事项This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
    背景资料BAALC is a 180 amino acid protein that localizes to both the membrane and the cytoplasm and exists as multiple alternatively spliced isoforms. Expressed by hematopoetic and neural cells, BAALC interacts with CaMKII and is thought to play a role in synaptic function at postsynaptic lipid rafts. BAALC may be overexpressed in acute myeloid leukemia (AML), suggesting a role in tumorigenesis. The gene encoding BAALC maps to human chromosome 8, which consists of nearly 146 million base pairs, houses more than 800 genes and is associated with a variety of diseases and malignancies. Schizophrenia, bipolar disorder, Trisomy 8, Pfeiffer syndrome, congenital hypothyroidism, Waardenburg syndrome and some leukemias and lymphomas are thought to occur as a result of defects in specific genes that maps to chromosome 8.

     

     

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