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SPG7 antibody (AA 1-250)

This anti-SPG7 antibody is a Rabbit Polyclonal antibody detecting SPG7 in WB and IHC. Suitable for Human.
Catalog No. ABIN6148342

Quick Overview for SPG7 antibody (AA 1-250) (ABIN6148342)

Target

See all SPG7 Antibodies
SPG7 (Spastic Paraplegia 7 (SPG7))

Reactivity

  • 23
  • 3
  • 3
  • 2
  • 1
  • 1
Human

Host

  • 16
  • 10
Rabbit

Clonality

  • 18
  • 8
Polyclonal

Conjugate

  • 21
  • 1
  • 1
  • 1
  • 1
  • 1
This SPG7 antibody is un-conjugated

Application

  • 24
  • 10
  • 10
  • 5
  • 4
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Binding Specificity

    • 7
    • 6
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-250

    Sequence

    MAVLLLLLRA LRRGPGPGPR PLWGPGPAWS PGFPARPGRG RPYMASRPPG DLAEAGGRAL QSLQLRLLTP TFEGINGLLL KQHLVQNPVR LWQLLGGTFY FNTSRLKQKN KEKDKSKGKA PEEDEEERRR RERDDQMYRE RLRTLLVIAV VMSLLNALST SGGSISWNDF VHEMLAKGEV QRVQVVPESD VVEVYLHPGA VVFGRPRLAL MYRMQVANID KFEEKLRAAE DELNIEAKDR IPVSYKRTGF

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-250 of human SPG7 (NP_003110.1).

    Isotype

    IgG
  • Application Notes

    WB,1:1000 - 1:2000,IHC,1:50 - 1:200

    Comment

    HIGH QUALITY

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    SPG7 (Spastic Paraplegia 7 (SPG7))

    Alternative Name

    SPG7

    Background

    This gene encodes a mitochondrial metalloprotease protein that is a member of the AAA family. Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis. Mutations in this gene cause autosomal recessive spastic paraplegia 7. Two transcript variants encoding distinct isoforms have been identified.,SPG7,CAR,CMAR,PGN,SPG5C,Cell Biology & Developmental Biology,Ubiquitin,Neuroscience,Neurodegenerative Diseases,SPG7

    Molecular Weight

    53 kDa/88 kDa

    Gene ID

    6687

    UniProt

    Q9UQ90
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