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TCN2 Protein (His tag)

This Recombinant TCN2 protein is produced in CHO Cells.
Catalog No. ABIN7317824

Quick Overview for TCN2 Protein (His tag) (ABIN7317824)

Target

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

Protein Type

Recombinant

Origin

  • 5
  • 2
  • 1
  • 1
  • 1
Human

Source

  • 3
  • 3
  • 2
  • 2
CHO Cells

Purity

> 90 % as determined by reducing SDS-PAGE.
  • Purification tag / Conjugate

    This TCN2 protein is labelled with His tag.

    Purpose

    Recombinant Human TCN2 Protein (His Tag)

    Sequence

    Met 1-Trp 427

    Characteristics

    A DNA sequence encoding the human TCN2 (NP_000346.2) (Met 1-Trp 427) was expressed with a C-terminal polyhistidine tag.

    Endotoxin Level

    < 1.0 EU per μg 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: Transcobalamin-II,D22S676,D22S750,II,TC,TC-2,TC2,TCII

    Molecular Weight

    46.7 kDa

    NCBI Accession

    NP_000346
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