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Mouse Monoclonal KID antibody [5F3] (STJ98196)
Supplier: St John’s Laboratory Ltd.
Recommended applications: WB, IHC, ELISA
Recommended dilution: WB 1:500-1:2000; IHC 1:200-1:1000; ELISA 1:10000
Recommended protocols: check protocols
Click or hover above images to see image description for KID Monoclonal Antibody.
Check alternative names for the antibodyExpand
KIF22 antibody, KID antibody, KNSL4 antibody,|A 328A3.2 antibody|KID antibody|KIF 22 antibody|kif22 antibody|KIF22_HUMAN antibody|Kinesin family member 22 antibody|Kinesin like 4 antibody|Kinesin like DNA binding protein antibody|Kinesin like DNA binding protein pseudogene antibody|Kinesin like protein 4 antibody|Kinesin like protein KIF22 antibody|Kinesin-like DNA-binding protein antibody|Kinesin-like protein 4 antibody|Kinesin-like protein KIF22 antibody|KNSL 4 antibody|KNSL4 antibody|OBP 1 antibody|OBP 2 antibody|OBP antibody|OBP1 antibody|OBP2 antibody|Origin of plasmid DNA replication binding protein antibody|OriP binding protein antibody|OTTHUMP00000123406 antibody|Anti-KIF22 antibody [EP2747Y] (ab75783)
SCBT cat No: sc-130645|sc-390640|sc-166814|sc-390533|sc-366118|
KID Monoclonal Antibody
|Catalogue No.|| |
KID Monoclonal Antibody detects endogenous levels of KID protein.
Purified recombinant fragment of human KID expressed in E Coli
WB, IHC, ELISA
|Recommended dilution|| |
WB 1:500-1:2000; IHC 1:200-1:1000; ELISA 1:10000
KID Antibody was tube-contained. Ascitic fluid containing 0.03% sodium azide.
KID Antibody was purified using affinity purification.
-20 Celsius degree. Avoid repeated freeze/thaw cycles.
|Alternative antibody names|| |
Kinesin-like protein KIF22 antibody, Kinesin-like DNA-binding protein antibody, Kinesin-like protein 4 antibody
|Protein names|| |
Kinesin-like protein KIF22 , Kinesin-like DNA-binding protein , Kinesin-like protein 4
|Protein function|| |
Kinesin family that is involved in spindle formation and the movements of chromosomes during mitosis and meiosis. Binds to microtubules and to DNA.
|Protein tissue specificity|| |
Expressed in bone, cartilage, joint capsule, ligament, skin, and primary cultured chondrocytes.
|Involvement in disease|| |
Spondyloepimetaphyseal dysplasia with joint laxity, 2 (SEMDJL2) [MIM:603546]: A bone disease characterized by short stature, distinctive midface retrusion, progressive knee malalignment (genu valgum and/or varum), generalized ligamentous laxity, and mild spinal deformity. Intellectual development is not impaired. Radiographic characteristics include significantly retarded epiphyseal ossification that evolves into epiphyseal dysplasia and precocious osteoarthritis, metaphyseal irregularities and vertical striations, constricted femoral neck, slender metacarpals and metatarsals, and mild thoracolumbar kyphosis or scoliosis with normal or mild platyspondyly. The most distinctive features for differential diagnosis of SEMDJL2 are the slender metacarpals and phalanges and the progressive degeneration of carpal bones; however, these 2 features are evident only in older children and young adults. The soft consistency of cartilage in the airways leads to laryngotracheomalacia with proneness to respiratory obstruction and inspiratory stridor in infancy and childhood. . Note: The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the TRAFAC class myosin-kinesin ATPase superfamily. Kinesin family. / Contains 1 kinesin motor domain.
|Protein post-translational modifications|| |
Ubiquitinated; mediated by SIAH1 and leading to its subsequent proteasomal degradation.
|Protein cellular localization|| |
Nucleus / Cytoplasm > cytoskeleton
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St John’s Laboratory Ltd.
|Product type|| |
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