Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

SPG7 antibody (AA 71-120)

This Rabbit Polyclonal antibody specifically detects SPG7 in WB and ELISA. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN8124872
$385.00
Plus shipping costs $50.00
50 μL
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for SPG7 antibody (AA 71-120) (ABIN8124872)

Target

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

Reactivity

  • 27
  • 6
  • 4
  • 3
  • 1
  • 1
Human, Mouse, Rat

Host

  • 19
  • 11
Rabbit

Clonality

  • 21
  • 9
Polyclonal

Conjugate

  • 25
  • 1
  • 1
  • 1
  • 1
  • 1
This SPG7 antibody is un-conjugated

Application

  • 28
  • 13
  • 10
  • 6
  • 5
  • 4
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA
  • Binding Specificity

    • 7
    • 6
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 71-120

    Purpose

    SPG7 Antibody

    Specificity

    SPG7 Polyclonal Antibody detects endogenous levels of protein.

    Purification

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

    Immunogen

    Synthesized peptide derived from human protein . at AA range: 71-120

    Isotype

    IgG
  • Application Notes

    WB 1:500-2000 ELISA 1:5000-20000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Liquid in PBS containing 50 % glycerol, and 0.02 % sodium azide.

    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/1 year

    Expiry Date

    12 months
  • Target

    SPG7 (Spastic Paraplegia 7 (SPG7))

    Alternative Name

    SPG7

    Background

    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. [provided by RefSeq, Mar 2014],

    Gene Name: SPG7 CAR CMAR PGN

    Protein Name: Paraplegin (EC 3.4.24.-) (Spastic paraplegia 7 protein)

    Gene ID

    6687

    UniProt

    Q9UQ90
You are here:
Chat with us!