Leprecan Like Protein 1 蛋白 (LEPREL1)

LEPREL1 encodes a member of the prolyl 3-hydroxylase subfamily of 2-oxo-glutarate-dependent dioxygenases. 再加上,我们可以发LEPREL1 抗体 (25)LEPREL1 试剂盒 (6)和数多这个蛋白质的别的产品。

列出全部蛋白 基因 基因ID UniProt
LEPREL1 210530 Q8CG71
LEPREL1 288016 Q4KLM6
LEPREL1 55214 Q8IVL5
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Insect Cells His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 60 Days
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Insect Cells 小鼠 His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 60 Days
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酵母菌 大鼠 His tag   1 mg Log in to see 60至71个工作日
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大肠杆菌(E. Coli) 非结合性   100 μg Log in to see 11至18个工作日
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LEPREL1 蛋白 by Origin and Source

Origin 在表达 标记
Mouse (Murine)

Rat (Rattus)

Human ,

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Mouse (Murine) Leprecan Like Protein 1 (LEPREL1) interaction partners

  1. Altered collagen prolyl 3-hydroxylation is caused by loss of P3H2.

  2. prolyl 3-hydroxylation of type IV collagen (显示 COL4 蛋白) by P3H2 has an important function preventing maternal platelet aggregation in response to the early developing embryo

  3. P3H2 is responsible for the hydroxylation of collagen IV (显示 COL4 蛋白), which has the highest 3-hydroxyproline content of all collagens. It is thus possible that P3H2 mutations may lead to a disease with changes in basement membranes.

  4. Study found that all 3 mouse Leprecan (显示 LEPRE1 蛋白) genes Lepre1 (显示 LEPRE1 蛋白), leprel1 and leprel2 (显示 LEPREL2 蛋白) are expressed in the notochord; additionally, they are expressed in dorsal root ganglia, limb buds, branchial arches, and developing kidneys.

  5. This report characterizes expression of the P3H1 (显示 LEPRE1 蛋白), P3H2 and P3H3 (显示 LEPREL2 蛋白) genes in embryonic and adult mice.

Human Leprecan Like Protein 1 (LEPREL1) interaction partners

  1. Recessive LEPREL1 mutations should be recognized as part of the differential diagnosis of lens subluxation.

  2. LEPREL1 plays an important role in eye development and homozygous loss-of-function mutation of this gene can cause severely high myopia and early-onset cataract.

  3. mutation in LRPAP1 is associated with high myopia. Further studies are expected to evaluate the pathogenicity of the variants in CTSH, LEPREL1, ZNF644, SLC39A5, and SCO2.

  4. High myopia is caused by a mutation in LEPREL1, encoding prolyl 3-hydroxylase 2.

  5. P3H2 has preferred substrate sequences among the classes of 3Hyp sites in clade A collagen chains

  6. P3H2 is responsible for the hydroxylation of collagen IV (显示 COL4 蛋白), which has the highest 3-hydroxyproline content of all collagens. It is thus possible that P3H2 mutations may lead to a disease with changes in basement membranes.

  7. The restriction of silencing in P3H2 to breast carcinomas, and its association with oestrogen-receptor-positive cases, suggests that P3H2 may be a breast-cancer-specific tumour suppressor.

蛋白简介LEPREL1

蛋白简介

This gene encodes a member of the prolyl 3-hydroxylase subfamily of 2-oxo-glutarate-dependent dioxygenases. These enzymes play a critical role in collagen chain assembly, stability and cross-linking by catalyzing post-translational 3-hydroxylation of proline residues. Mutations in this gene are associated with nonsyndromic severe myopia with cataract and vitreoretinal degeneration, and downregulation of this gene may play a role in breast cancer. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.

Gene names and symbols associated with LEPREL1

  • prolyl 3-hydroxylase 2 (P3h2)
  • prolyl 3-hydroxylase 2 (P3H2)
  • 4832416N06 蛋白
  • AW553532 蛋白
  • MCVD 蛋白
  • MLAT4 蛋白
  • P3H2 蛋白

Protein level used designations for LEPREL1

leprecan-like protein 1 , myxoid liposarcoma associated protein 4 , prolyl 3-hydroxylase 2 , myxoid liposarcoma-associated protein 4 , prolyl 3-hydroxylase 3

GENE ID SPECIES
210530 Mus musculus
288016 Rattus norvegicus
55214 Homo sapiens
414143 Gallus gallus
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