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TCN2 Protein (His tag)

Recombinant TCN2 protein expressed in HEK-293 Cells.
Catalog No. ABIN7198283

Quick Overview for TCN2 Protein (His tag) (ABIN7198283)

Target

See all TCN2 Proteins
TCN2 (Transcobalamin II (TCN2))

Protein Type

Recombinant

Origin

  • 6
  • 2
  • 1
  • 1
Mouse

Source

  • 3
  • 3
  • 2
  • 1
  • 1
HEK-293 Cells

Purity

> 95 % as determined by SDS-PAGE
  • Purification tag / Conjugate

    This TCN2 protein is labelled with His tag.

    Purpose

    Recombinant Mouse TCN2 Protein (His Tag)

    Sequence

    Met 1-Trp 430

    Characteristics

    A DNA sequence encoding the mouse TCN2 (O88968) (Met 1-Trp 430) was expressed, with a C-terminal polyhistidine tag.

    Endotoxin Level

    < 1.0 EU per μg of the protein as determined by the LAL method.
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  • Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Please refer to the printed manual for detailed information.

    Buffer

    Lyophilized from sterile PBS, pH 7.4

    Storage

    4 °C,-20 °C,-80 °C

    Storage Comment

    Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80°C. Reconstituted protein solution can be stored at 4-8°C for 2-7 days. Aliquots of reconstituted samples are stable at < -20°C for 3 months.
  • Target

    TCN2 (Transcobalamin II (TCN2))

    Alternative Name

    TCN2

    Background

    Background: Transcobalamin II, also known as TCN2 and TC II, is a plasma protein that binds cobalamin (Cbl, vitamin B12) as it is absorbed in the terminal ileum and distributes to tissues. The circulating transcobalamin II-cobalamin complex binds to receptors on the plasma membrane of tissue cells and is then internalized by receptor-mediated endocytosis. Transcobalamin II is a non-glycolated secretory protein of molecular mass 43 kDa. Its plasma membrane receptor (TC II-R) is a heavily glycosylated protein with a monomeric molecular mass of 62 kDa. Human TCN2 gene is composed of nine exons and eight introns spanning approximately 20 kb with multiple potential transcription start sites. A number of genetic abnormalities are characterized either by a failure to express TCN2 or by synthesis of an abnormal protein. The TCN2 deficiency results in cellular cobalamin deficiency, an early onset of megaloblastic anaemia, and neurological abnormalities.

    Synonym: AW208754,Tcn-2

    Molecular Weight

    47 kDa

    UniProt

    O88968
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