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Magic™ Membrane Protein Human ATP2C1 (ATPase secretory pathway Ca2+ transporting 1) Full Length (CAT#: MPC1154K) Made to Order

Datasheet
This product is a 100.5 kDa Human ATP2C1 membrane protein expressed in HEK293. The protein is for research use only and is not approved for use in humans or in clinical diagnosis.

Product Specifications

  • Host Species
  • Human
  • Target Protein
  • ATP2C1
  • Protein Length
  • Full length
  • Protein Class
  • Transporter
  • Molecular Weight
  • 100.5 kDa
  • TMD
  • 10
  • Sequence
  • MKVARFQKIPNGENETMIPVLTSKKASELPVSEVASILQADLQNGLNKCE
    VSHRRAFHGWNEFDISEDEPLWKKYISQFKNPLIMLLLASAVISVLMHQF
    DDAVSITVAILIVVTVAFVQEYRSEKSLEELSKLVPPECHCVREGKLEHT
    LARDLVPGDTVCLSVGDRVPADLRLFEAVDLSIDESSLTGETTPCSKVTA
    PQPAATNGDLASRSNIAFMGTLVRCGKAKGVVIGTGENSEFGEVFKMMQA
    EEAPKTPLQKSMDLLGKQLSFYSFGIIGIIMLVGWLLGKDILEMFTISVS
    LAVAAIPEGLPIVVTVTLALGVMRMVKKRAIVKKLPIVETLGCCNVICSD
    KTGTLTKNEMTVTHIFTSDGLHAEVTGVGYNQFGEVIVDGDVVHGFYNPA
    VSRIVEAGCVCNDAVIRNNTLMGKPTEGALIALAMKMGLDGLQQDYIRKA
    EYPFSSEQKWMAVKCVHRTQQDRPEICFMKGAYEQVIKYCTTYQSKGQTL
    TLTQQQRDVYQQEKARMGSAGLRVLALASGPELGQLTFLGLVGIIDPPRT
    GVKEAVTTLIASGVSIKMITGDSQETAVAIASRLGLYSKTSQSVSGEEID
    AMDVQQLSQIVPKVAVFYRASPRHKMKIIKSLQKNGSVVAMTGDGVNDAV
    ALKAADIGVAMGQTGTDVCKEAADMILVDDDFQTIMSAIEEGKGIYNNIK
    NFVRFQLSTSIAALTLISLATLMNFPNPLNAMQILWINIIMDGPPAQSLG
    VEPVDKDVIRKPPRNWKDSILTKNLILKILVSSIIIVCGTLFVFWRELRD
    NVITPRDTTMTFTCFVFFDMFNALSSRSQTKSVFEIGLCSNRMFCYAVLG
    SIMGQLLVIYFPPLQKVFQTESLSILDLLFLLGLTSSVCIVAEIIKKVER
    SREKIQKHVSSTSSSFLEV

Product Description

  • Expression Systems
  • HEK293
  • Tag
  • Flag-StrepII or based on specific requirements
  • Protein Format
  • Detergent or based on specific requirements

Target

  • Target Protein
  • ATP2C1
  • Full Name
  • ATPase secretory pathway Ca2+ transporting 1
  • Introduction
  • The protein encoded by this gene belongs to the family of P-type cation transport ATPases. This magnesium-dependent enzyme catalyzes the hydrolysis of ATP coupled with the transport of calcium ions. Defects in this gene cause Hailey-Hailey disease, an autosomal dominant disorder. Alternatively spliced transcript variants encoding different isoforms have been identified.
  • Alternative Names
  • ATP2C1; HHD; BCPM; PMR1; SPCA1; hSPCA1; ATP2C1A; calcium-transporting ATPase type 2C member 1; ATP-dependent Ca(2+) pump PMR1; ATPase 2C1; ATPase, Ca(2+)-sequestering; ATPase, Ca++ transporting, type 2C, member 1; HUSSY-28; secretory pathway Ca2+/Mn2+ ATPase 1; ATPase secretory pathway Ca2+ transporting 1

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