KIF22 Recombinant Monoclonal Antibody
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中文名稱:KIF22 Recombinant Monoclonal Antibody
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貨號:CSB-RA144792A0HU
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規格:¥1320
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圖片:
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其他:
產品詳情
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Uniprot No.:
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基因名:KIF22
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別名:KIF22; Kinesin Family Member 22; OBP-1; OBP-2; KNSL4; Kid; Kinesin-Like Protein KIF22; Kinesin-Like Protein 4; Origin Of Plasmid DNA Replication-Binding Protein; Kinesin-Like DNA-Binding Protein Pseudogene; Kinesin-Like DNA-Binding Protein; OriP Binding Protein; Kinesin-Like 4; A-328A3.2; SEMDJL2; OBP; KID
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反應種屬:Human
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免疫原:Recombinant Human KIF22 protein
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免疫原種屬:Homo sapiens (Human)
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標記方式:Non-conjugated
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克隆類型:Monoclonal
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抗體亞型:Rabbit IgG
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純化方式:Affinity-chromatography
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克隆號:12F10
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濃度:It differs from different batches. Please contact us to confirm it.
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保存緩沖液:Rabbit IgG in PBS (pH 7.4) containing 50% glycerol, and 0.02% sodium azide.
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產品提供形式:Liquid
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應用范圍:ELISA, WB
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推薦稀釋比:
Application Recommended Dilution WB 1:1000-1:5000 -
Protocols:
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儲存條件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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貨期:Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
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用途:For Research Use Only. Not for use in diagnostic or therapeutic procedures.
相關產品
靶點詳情
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功能:Kinesin family member that is involved in spindle formation and the movements of chromosomes during mitosis and meiosis. Binds to microtubules and to DNA. Plays a role in congression of laterally attached chromosomes in NDC80-depleted cells.
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基因功能參考文獻:
- Chromokinesin Kid and kinetochore kinesin CENP-E differentially support chromosome congression without end-on attachment to microtubules. PMID: 25743205
- we conclude that inhibition of KIF22 suppresses cancer cell proliferation by delaying mitotic exit through the transcriptional upregulation of CDC25C. PMID: 24626146
- Whole-exome sequencing identifies mutations of KIF22 in spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type PMID: 22152677
- Recurrent dominant mutations affecting two adjacent residues in the motor domain of the monomeric kinesin KIF22 result in skeletal dysplasia and joint laxity PMID: 22152678
- in all breast tumor tissues analyzed, variations in the Kid/KIF22 mRNA levels mirrored those seen with SIAH-1 mRNAs. PMID: 20144232
- These results are consistent with Kid having a role in chromosome congression in vivo, where it would be responsible for the polar ejection forces acting on the chromosome arms. PMID: 12606572
- its molecular structure and interaction with microtubules PMID: 12692123
- These results suggest that distinct from its role in chromosome movement, Kid contributes to spindle morphogenesis by mediating spindle microtubules stabilization. PMID: 16176979
- human Aurora B and Kid are identified as APC/C(Cdh1) substrates PMID: 17726374
- Association of importin-beta and -alpha with hKid triggers the initial targeting of hKid to mitotic chromosomes; local Ran-GTP-mediated cargo release promotes the accumulation of hKid on chromosomes. PMID: 18268099
- These data suggest that Kid-mediated anaphase/telophase chromosome compaction prevents formation of multinucleated cells. PMID: 18329364
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相關疾病:Spondyloepimetaphyseal dysplasia with joint laxity, 2 (SEMDJL2)
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亞細胞定位:Nucleus. Cytoplasm, cytoskeleton.
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蛋白家族:TRAFAC class myosin-kinesin ATPase superfamily, Kinesin family
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組織特異性:Expressed in bone, cartilage, joint capsule, ligament, skin, and primary cultured chondrocytes.
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數據庫鏈接:
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