Recombinant Human Membrane-associated phosphatidylinositol transfer protein 3 (PITPNM3), partial, Homo sapiens (Human), E.coli, N-terminal 10xHis-tagged and C-terminal Myc-tagged, 30.8kDa, purity >90% as determined by SDS-PAGE.

Recombinant Human Membrane-associated phosphatidylinositol transfer protein 3 (PITPNM3), partial

Recombinant Human Membrane-associated phosphatidylinositol transfer protein 3 (PITPNM3), partial — Catalyzes the transfer of phosphatidylinositol and phosphatidylcholine between membranes (in vitro). Purity >90%.

SKU: BCRECP-001387 Category:
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Product Specifications

Product SkuBCRECP-001387
Product DescriptionRecombinant Human Membrane-associated phosphatidylinositol transfer protein 3 (PITPNM3) Protein is expressed from E.coli with N-terminal 10xHis-tagged and C-terminal Myc-tagged. It contains 387-597aa. [Accession | Q9BZ71].
Uniprot No.Q9BZ71
Gene NamesPITPNM3
PurityGreater than 90% as determined by SDS-PAGE.
Expression SystemE.coli
Expression Region387-597aa
SpeciesHomo sapiens (Human)
Tag InfoN-terminal 10xHis-tagged and C-terminal Myc-tagged
Molecular weight30.8kDa
ActivityPlease contact us to obtain bioactivity data.
BufferIf the delivery form is liquid, the default storage buffer is Tris/PBS-based buffer, 5%-50% glycerol. If the delivery form is lyophilized powder, the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose.
StorageStore at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles.
Research AreasNeuroscience

Function

Catalyzes the transfer of phosphatidylinositol and phosphatidylcholine between membranes (in vitro). Binds calcium ions.

Biological Context

Subcellular Location: Endomembrane system (Peripheral membrane protein)
Tissue Specificity: Detected in brain and spleen, and at low levels in ovary
Disease Association: Cone-rod dystrophy 5 (CORD5) : An inherited retinal dystrophy characterized by retinal pigment deposits visible on fundus examination, predominantly in the macular region, and initial loss of cone photoreceptors followed by rod degeneration. This leads to decreased visual acuity and sensitivity in the central visual field, followed by loss of peripheral vision. Severe loss of vision occurs earlier than in retinitis pigmentosa, due to cone photoreceptors degenerating at a higher rate than rod photoreceptors. [The disease is caused by variants affecting the gene represented in this entry]

Product Specifications

Recombinant Human Membrane-associated phosphatidylinositol transfer protein 3 (PITPNM3), partial is a recombinant protein from Homo sapiens (Human), expressed in E.coli, covering amino acids 387-597aa, with N-terminal 10xHis-tagged and C-terminal Myc-tagged tag, molecular weight 30.8kDa, purity Greater than 90% as determined by SDS-PAGE.. Suitable for ELISA and Western Blot applications.

Recommended applications depend on the target, product format, and product-specific validation data. Refer to the product datasheet or Certificate of Analysis (CoA), or contact BioCrest Sci for application guidance.

Biological Activity: Please contact us to obtain bioactivity data.

Storage: Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles.

Shipping & Lead Time: Availability, shipping conditions, and estimated lead time are confirmed in the formal quotation or order confirmation based on the product format, destination, and order requirements.

Related products

Protein Biology

Function

Catalyzes the transfer of phosphatidylinositol and phosphatidylcholine between membranes (in vitro) (By similarity). Binds calcium ions

Subcellular Location

Endomembrane system (Peripheral membrane protein)

Disease Association

Cone-rod dystrophy 5 (CORD5) : An inherited retinal dystrophy characterized by retinal pigment deposits visible on fundus examination, predominantly in the macular region, and initial loss of cone photoreceptors followed by rod degeneration. This leads to decreased visual acuity and sensitivity in the central visual field, followed by loss of peripheral vision. Severe loss of vision occurs earlier than in retinitis pigmentosa, due to cone photoreceptors degenerating at a higher rate than rod photoreceptors. [The disease is caused by variants affecting the gene represented in this entry]

Tissue Specificity

Detected in brain and spleen, and at low levels in ovary

Subunit

Interacts with PTK2B via its C-terminus

Gene: PITPNM3  |  Organism: Homo sapiens  |  Synonyms: Phosphatidylinositol transfer protein, membrane-associated 3; Pyk2 N-terminal domain-interacting receptor 1
Key Publications

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Submit the Online Inquiry form with your required quantity and specifications, or email sales@biocrestsci.com. Available sizes, pricing, stock status, documentation, and estimated lead time are confirmed in the formal quotation.

What is the shipping and delivery time?

Availability, dispatch timing, shipping conditions, and delivery estimates depend on the product format, destination, and order requirements. These details are confirmed in the formal quotation or order confirmation.

How should this product be stored?

Follow the storage and handling instructions in the product-specific datasheet and Certificate of Analysis (CoA). Requirements may vary by product form and formulation; contact BioCrest Sci if product-specific guidance is needed.

What quality controls are performed on your products?

Quality-control data such as identity, purity, endotoxin level, or biological activity are provided only when specified on this product page, the datasheet, or Certificate of Analysis (CoA). Biological activity is not implied unless explicitly stated.

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