SPG7 antibody (AA 71-120)

Catalog No. ABIN7231494

This anti-SPG7 antibody is a Rabbit Polyclonal antibody detecting SPG7 in WB and ELISA. Suitable for Human.

Quick Overview for SPG7 antibody (AA 71-120) (ABIN7231494)

Target: SPG7 (Spastic Paraplegia 7 (SPG7))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SPG7 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-SPG7 Antibody

Binding Specificity: AA 71-120

Purpose: SPG7 Polyclonal Antibody

Specificity: The antibody detects endogenous levels of SPG7 protein

Purification: The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

Immunogen: Synthesized peptide derived from part region of human SPG7 protein at AA range: 71-120

Isotype: IgG

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

Comment:

Primary Antibody

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

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: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Target Details for SPG7

Target: SPG7 (Spastic Paraplegia 7 (SPG7))

Alternative Name: SPG7

Background: Rabbit Anti-SPG7 Polyclonal Antibody,Paraplegin, Cell matrix adhesion regulator, Spastic paraplegia 7 protein,SPG7 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 SPG7 cause autosomal recessive spastic paraplegia 7. Two transcript variants encoding distinct isoforms have been identified.,SPG7

Molecular Weight: observerd band 87kDa

Gene ID: 6687

UniProt: Q9UQ90