BFSP1 (Human) Recombinant Protein (Q01)

Catalog # H00000631-Q01

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Size:25 ug
Price: USD $ 510.00
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Size:10 ug
Price: USD $ 335.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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  • Specification

    Product Description

    Human BFSP1 partial ORF ( NP_001186, 567 a.a. - 664 a.a.) recombinant protein with GST-tag at N-terminal.

    Sequence

    EESRRPCAMVTPGAEEPSIPEPPKPAADQDGAEVLGTRSRSLPEKGPPKALAYKTVEVVESIEKISTESIQTYEETAVIVETMIGKTKSDKKKSGEKS

    Host

    Wheat Germ (in vitro)

    Theoretical MW (kDa)

    36.52

    Interspecies Antigen Sequence

    Mouse (60); Rat (60)

    Preparation Method

    in vitro wheat germ expression system

    Purification

    Glutathione Sepharose 4 Fast Flow

    Quality Control Testing

    12.5% SDS-PAGE Stained with Coomassie Blue.

    Storage Buffer

    50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.

    Storage Instruction

    Store at -80°C. Aliquot to avoid repeated freezing and thawing.

    Note

    Best use within three months from the date of receipt of this protein.

  • Applications

    Enzyme-linked Immunoabsorbent Assay

    Western Blot (Recombinant protein)

    Antibody Production

    Protein Array

  • Gene Info — BFSP1

    Entrez GeneID

    631

    GeneBank Accession#

    NM_001195

    Protein Accession#

    NP_001186

    Gene Name

    BFSP1

    Gene Alias

    CP115, CP94, FILENSIN, LIFL-H

    Gene Description

    beaded filament structural protein 1, filensin

    Omim ID

    603307 611391

    Gene Ontology

    Hyperlink

    Gene Summary

    More than 99% of the vertebrate ocular lens is comprised of terminally differentiated lens fiber cells. Two lens-specific intermediate filament-like proteins, CP49 (also known as phakinin) and the protein product of this gene, filensin, are expressed only after fiber cell differentiation has begun. Both proteins are found in a structurally unique cytoskeletal element that is referred to as the beaded filament (BF). Mutations in this gene are the cause of autosomal recessive cortical juvenile-onset cataract. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq

    Other Designations

    OTTHUMP00000030329|cytoskeletal protein, 115 KD|filensin

  • Interactome
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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