anti-Major Intrinsic Protein of Lens Fiber (MIP) 抗体

Major intrinsic protein is a member of the water-transporting aquaporins as well as the original member of the MIP family of channel proteins. 再加上,我们可以发MIP 试剂盒 (16)和数多这个蛋白质的别的产品。

列出全部抗体 基因 基因ID UniProt
MIP 17339 P51180
MIP 4284 P30301
MIP 25480  

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Showing 10 out of 47 products:

产品编号 适用 宿主 标记 应用范围 图像 规格 供应商 交付 价格 详细
非结合性 WB Western blot analysis of Aquaporin 0 expression in HeLa (A), SP2/0 (B), PC12 (C) whole cell lysates. 200 μL Log in to see 7至8个工作日
¥3,941.44
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非结合性 ELISA, IHC, WB 100 μL Log in to see 34至38个工作日
¥4,371.67
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非结合性 IHC (p), WB Immunohistochemistry analyzes of AP20629PU-N AQP0 antibody in paraffin-embedded human brain tissue. Western blot analysis of AP20629PU-N AQP0 antibody in extracts from HT-29 cells. 0.1 mg Log in to see 29至35个工作日
¥3,884.46
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非结合性 WB Western blot analysis of extracts of mouse eyes tissue lysate, using MIP antibody. 100 μL Log in to see 34至38个工作日
¥2,882.69
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Alexa Fluor 350 IF (p)   100 μL Log in to see 14至17个工作日
¥3,555.98
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Alexa Fluor 488 IF (p)   100 μL Log in to see 14至17个工作日
¥3,555.98
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Alexa Fluor 555 IF (p)   100 μL Log in to see 14至17个工作日
¥3,555.98
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Alexa Fluor 594 IF (p)   100 μL Log in to see 14至17个工作日
¥3,555.98
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Alexa Fluor 647 IF (p)   100 μL Log in to see 14至17个工作日
¥3,555.98
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Cy3 IF (p)   100 μL Log in to see 14至17个工作日
¥3,555.98
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通过反应活性、应用领域、克隆类型和共轭标记 MIP 抗体

特性 应用范围 宿主 克隆类型 标记
Mouse (Murine) ,


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更多抗MIP的相互作用对抗体

Xenopus laevis Major Intrinsic Protein of Lens Fiber (MIP) interaction partners

  1. The proposed schematic models illustrate that cell-to-cell adhesion elicited by AQP0 is vital for lens transparency and homeostasis.

  2. A concentration signal could trigger a regulatory change in AQP0 water permeability.

Mouse (Murine) Major Intrinsic Protein of Lens Fiber (MIP) interaction partners

  1. Cataractogenesis in Mip(Nat (显示 BRD2 抗体)) mutants are caused by defects in MIP expression.

  2. These data suggest that while relatively few genes ( approximately 1.5% of the transcriptome) were differentially regulated >2-fold in the Mip-/- lens, calpain hyper-activation acts as a terminal pathogenic event during lens fiber cell death and cataract formation.

  3. hypothesize that AQP0, with its prolific expression at the fiber cell membrane, could provide anchorage for cytoskeletal structures like BFs and together they help to confer fiber cell shape, architecture and integrity

  4. In summary, lens transparency, CTCA and compact packing of fiber cells were affected due to the loss of 50% AQP0 leading to larger extracellular space, more water content and SA, possibly due to alteration in RING.

  5. Post-translational truncation of N- or C-terminal end amino acids does not alter the basal water permeability of AQP0 or its adhesive functions.

  6. Data show that Ca(V) 1.2 and 1.3 channels are expressed in lens, regulating phosphorylation of aquaporin-0 and myosin light chain and expression of connexins 50 and 46.

  7. The additional negative charge introduced by phosphoserine 235 perturbs electrostatic interactions between aquaporin-0 and calmodulin (显示 Calm2 抗体) to favour water influx through the channel.

  8. increased water permeability through AQP1 (显示 AQP1 抗体) does not compensate for loss of AQP0 expression in TgAQP1(+/+)/AQP0(-/-) mice. Fiber cell AQP0 expression is required to maintain their organization, which is a requisite for lens transparency

  9. Kynurenine might inhibit FGF2 (显示 FGF2 抗体)-mediated fiber cell differentiation by preventing expression of crystallins and MIP26.

  10. MIP has essential roles in the establishment and maintenance of uniform fiber structure, and the organization of fibers, and as such is essential for lens function.

Human Major Intrinsic Protein of Lens Fiber (MIP) interaction partners

  1. The data evidence a broad lipidation profile of AQP0 that is both species and site independent, suggesting a chemical-based ester aminolysis mechanism to explain such modifications.

  2. A novel MIP (显示 TNPO1 抗体) frame-shift mutation in familial congenital nuclear cataract patient

  3. defects in AQP-0 permeability may be a cause for presbyopia.

  4. the p.D150H mutation is a novel disease-causing mutation in MIP (显示 TNPO1 抗体), which leads to congenital progressive cortical punctate cataract by impairing the trafficking mechanism of AQP0.

  5. Authors identified a novel nonsense mutation in MIP (显示 TNPO1 抗体) (c.657 C>G; p.Y219*) (major intrinsic protein gene) that segregates with congenital posterior polar cataract in a Chinese family.

  6. Functional evidence linking the new MIP (显示 TNPO1 抗体) mutation of G215D to autosomal dominant congenital cataracts.

  7. A novel donor splice-site mutation (c.606+1G>A) in the MIP (显示 TNPO1 抗体) gene causes congenital cataract in a Chinese family.

  8. the first nonsense mutation of MIP (显示 TNPO1 抗体) identified in autosomal dominant congenital cataracts

  9. Mutation of this conserved glycine residue leads to improper trafficking of AQP0-G165D and loss of water channel (显示 AQP4 抗体) function.

  10. Aquaporin 0 R233K mutation did not affect the expression, location and trafficking of the protein but did influence the interaction between AQP0 and CaM (显示 CALM1 抗体).

Cow (Bovine) Major Intrinsic Protein of Lens Fiber (MIP) interaction partners

  1. The data evidence a broad lipidation profile of AQP0 that is both species and site independent, suggesting a chemical-based ester aminolysis mechanism to explain such modifications.

  2. In the presence of alpha-crystallin, this conversion to beta-sheet is minimized, suggesting that the protein structure that binds to the molecular chaperone (显示 HSP90AA1 抗体) is mostly the alpha-helical structure of AQP0.

  3. Determined the pseudoatomic structure of full-length aquaporin-0 (AQP0) in complex with calmodulin (显示 KRIT1 抗体), using electron microscopy to elucidate how this signaling protein modulates water-channel (显示 AQP4 抗体) function.

  4. Tyr23 is a dominate factor leading to the low water permeability in AQP0.

  5. AQP-0 and connexins can be segregated in the membrane by protein-lipid interactions as modified by AQP-0 homo-oligomerization

  6. determination of the x-ray structure of bovine aquaporin 0 to a resolution of 2.2 A; structure aids the analysis of the interaction of the extracellular domains and the possibility of a cell-cell adhesion role for AQP0

  7. The crystal packing was determined by molecular replacement and shows that, within the cubic lattice, AQP0 tetramers are associated head-to-head along their 4-fold axes.

MIP 抗原简介

蛋白简介

Major intrinsic protein is a member of the water-transporting aquaporins as well as the original member of the MIP family of channel proteins. The function of the fiber cell membrane protein encoded by this gene is undetermined, yet this protein is speculated to play a role in intracellular communication. The MIP protein is expressed in the ocular lens and is required for correct lens function. This gene has been mapped among aquaporins AQP2, AQP5, and AQP6, in a potential gene cluster at 12q13.

Gene names and symbols associated with MIP

  • major intrinsic protein of lens fiber (mip) 抗体
  • major intrinsic protein of lens fiber (MIP) 抗体
  • major intrinsic protein of eye lens fiber (Mip) 抗体
  • major intrinsic protein of lens fiber (Mip) 抗体
  • AQP0 抗体
  • Cat 抗体
  • CTRCT15 抗体
  • Hfi 抗体
  • LIM1 抗体
  • Lop 抗体
  • MIP 抗体
  • MIP26 抗体
  • MP22 抗体
  • MP26 抗体
  • shrivelled 抗体
  • Svl 抗体

Protein level used designations for MIP

major intrinsic protein of lens fiber , aquaporin 0 , MP26 , aquaporin-0 , dominant cataract , hydropic fibers , lens fiber major intrinsic protein , lens opacity , MIP26 , major intrinsic protein of eye lens fiber , AQP0 , aquaporin , Aquaporin-0

GENE ID SPECIES
495140 Xenopus laevis
100037914 Xenopus (Silurana) tropicalis
712901 Macaca mulatta
747083 Pan troglodytes
17339 Mus musculus
100135575 Cavia porcellus
4284 Homo sapiens
25480 Rattus norvegicus
374124 Gallus gallus
280859 Bos taurus
100101574 Oryctolagus cuniculus
607104 Canis lupus familiaris
100294602 Ovis aries
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