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CA2 Protein (AA 1-260)

This Recombinant CA2 protein is expressed in Escherichia coli (E. coli).
Catalog No. ABIN667740

Quick Overview for CA2 Protein (AA 1-260) (ABIN667740)

Target

See all CA2 Proteins
CA2 (Carbonic Anhydrase II (CA2))

Protein Type

Recombinant

Biological Activity

Active

Origin

  • 12
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
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  • 1
Human

Source

  • 19
  • 7
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Escherichia coli (E. coli)

Application

SDS-PAGE (SDS), Enzyme Activity Assay (EAA)

Purity

> 95 %
  • Protein Characteristics

    AA 1-260

    Sequence

    MSHHWGYGKH NGPEHWHKDF PIAKGERQSP VDIDTHTAKY DPSLKPLSVS YDQATSLRIL NNGHAFNVEF DDSQDKAVLK GGPLDGTYRL IQFHFHWGSL DGQGSEHTVD KKKYAAELHL VHWNTKYGDF GKAVQQPDGL AVLGIFLKVG SAKPGLQKVV DVLDSIKTKG KSADFTNFDP RGLLPESLDY WTYPGSLTTP PLLECVTWIV LKEPISVSSE QVLKFRKLNF NGEGEPEELM VDNWRPAQPL KNRQIKASFK

    Characteristics

    Carbonic anhydrase 2 , 1-260aa, Human, Recombinant, E.coli

    Purification

    > 95% by SDS-PAGE

    Biological Activity Comment

    Specific activity is > 7,000pmol/min/ug, and is defined as the amount of enzyme that hydrolyze 1.0pmole of 4-nitrophenyl acetate to 4-nitrophenol per minute at pH 8.0 at 37C.
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  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    Phosphate-Buffered Saline ( pH 7.4) containing 10 % glycerol

    Storage

    4 °C,-20 °C,-80 °C

    Storage Comment

    Can be stored at +2C to +8C for 1 week. For long term storage, aliquot and store at -20C to -80C. Avoid repeated freezing and thawing cycles.
  • Target

    CA2 (Carbonic Anhydrase II (CA2))

    Alternative Name

    Carbonic Anhydrase 2/CA2

    Background

    Carbonic anhydrase 2 (CA2) is one of fourteen forms of human alpha carbonic anhydrases. Carbonic anhydrase catalyzes reversible hydration of carbon dioxide. CA2 is a cytosolic enzyme with the highest activity among all known CAs. Mutations in the CA2 gene result in the CA2 deficiency syndrome, an autosomal recessive disorder that produces osteopetrosis, renal tubular acidosis and cerebral calcification. Recombinant human CA2 was expressed in E. coli and purified by using conventional chromatography.

    Molecular Weight

    29.2 kDa (260aa) confirmed by MALDI-TOF

    NCBI Accession

    NP_000058
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