Rabbit anti-Human SPG7 Polyclonal Antibody | anti-SPG7 antibody

SPG7, ID (SPG7, CAR, CMAR, PGN, Paraplegin, Spastic paraplegia 7 protein)

Cat. Num. AAA645956

• Gene Names: SPG7; CAR; PGN; CMAR; SPG5C
• Reactivity: Human
• Applications: ELISA, Western Blot, Immunohistochemistry
• Purity: Affinity Purified; Purified by Protein A affinity chromatography.
• Synonyms: SPG7; Polyclonal Antibody; ID (SPG7; CAR; CMAR; PGN; Paraplegin; Spastic paraplegia 7 protein); Anti -SPG7; anti-SPG7 antibody

• Host: Rabbit
• Reactivity: Human
• Clonality: Polyclonal
• Isotype: IgG
• Specificity: Human
• Purity/Purification: Affinity Purified; Purified by Protein A affinity chromatography.
• Form/Format: Supplied as a liquid in PBS, pH 7.2, 0.09% sodium azide.

• Applicable Applications for anti-SPG7 antibody: ELISA (EL/EIA), Western Blot (WB), Immunohistochemistry (IHC)
• Application Notes: Suitable for use in Western Blot, Immunohistochemistry, ELISA; Dilution: ELISA: 1:1,000; Western Blot: 1:100-500; Immunohistochemistry: 1:10-50
• Immunogen: SPG7 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 114-141 amino acids from the Central region of human SPG7.
• Preparation and Storage: May be stored at 4 degree C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20 degree C. Aliquots are stable for 12 months. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.

Western Blot (WB)

(SPG7 Antibody (Center) western blot analysis in 293 cell line lysates (35ug/lane).This demonstrates the SPG7 antibody detected the SPG7 protein (arrow).)

Immunohistochemistry (IHC)

(SPG7 Antibody (Center) immunohistochemistry analysis in formalin fixed and paraffin embedded human brain tissue followed by peroxidase conjugation of the secondary antibody and DAB staining.This data demonstrates the use of SPG7 Antibody (Center) for immunohistochemistry. Clinical relevance has not been evaluated.)

Related Product Information for anti-SPG7 antibody

This gene encodes a nuclear-encoded mitochondrial metalloprotease protein that is a member of the AAA (ATPases associated with a variety of cellular activities) protein 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. Two transcript variants encoding distinct isoforms have been identified for this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 7. [provided by RefSeq].

Product Categories/Family for anti-SPG7 antibody

Antibodies; Abs to Proteins

NCBI and Uniprot Product Information

• NCBI GI #: 34783526
• NCBI GeneID: 6687
• UniProt Accession #: Q9UQ90; O75756; Q2TB70; Q58F00; Q96IB0
• Molecular Weight: 88,235 Da
• NCBI Official Full Name: SPG7 protein
• NCBI Official Synonym Full Names: spastic paraplegia 7 (pure and complicated autosomal recessive)
• NCBI Official Symbol: SPG7
• NCBI Official Synonym Symbols: CAR; PGN; CMAR; SPG5C
• NCBI Protein Information: paraplegin; paraplegin, isoform 1; cell adhesion regulator; spastic paraplegia 7 protein; cell matrix adhesion regulator
• UniProt Protein Name: Paraplegin
• Protein Family: Paraplegin
• UniProt Gene Name: SPG7
• UniProt Synonym Gene Names: CAR; CMAR; PGN
• UniProt Entry Name: SPG7_HUMAN

NCBI Description

This gene encodes a nuclear-encoded mitochondrial metalloprotease protein that is a member of the AAA (ATPases associated with a variety of cellular activities) protein 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. Two transcript variants encoding distinct isoforms have been identified for this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 7. [provided by RefSeq, Jul 2008]

Uniprot Description

Function: Putative ATP-dependent zinc metalloprotease.

Subunit structure: Interacts with AFG3L2; the interaction is required for the efficient assembly of mitochondrial complex I. Ref.4

Subcellular location: Mitochondrion membrane; Multi-pass membrane protein Ref.1.

Tissue specificity: Ubiquitous.

Involvement in disease: Spastic paraplegia 7, autosomal recessive (SPG7) [MIM:607259]: A form of spastic paraplegia, a neurodegenerative disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. Rate of progression and the severity of symptoms are quite variable. Initial symptoms may include difficulty with balance, weakness and stiffness in the legs, muscle spasms, and dragging the toes when walking. In some forms of the disorder, bladder symptoms (such as incontinence) may appear, or the weakness and stiffness may spread to other parts of the body. SPG7 is a complex form. Additional clinical features are cerebellar syndrome, supranuclear palsy, and cognitive impairment, particularly disturbance of attention and executive functions.Note: The disease is caused by mutations affecting the gene represented in this entry. Ref.1 Ref.7 Ref.8 Ref.9Defects in SPG7 may cause autosomal recessive osteogenesis imperfecta (OI). Osteogenesis imperfecta defines a group of connective tissue disorders characterized by bone fragility and low bone mass. Clinical features of SPG7-related osteogenesis imperfecta include recurrent fractures, mild bone deformities, delayed tooth eruption, normal hearing and white sclera.

Sequence similarities: In the N-terminal section; belongs to the AAA ATPase family.In the C-terminal section; belongs to the peptidase M41 family.

Caution: A CDS in the 3'-UTR of SPG7 mRNA had been erroneously identified as a cell matrix adhesion regulator and originally thought to be encoded by the CMAR gene. There is no experimental evidence for the production of endogenous CMAR protein.

Sequence caution: The sequence AAH35929.1 differs from that shown. Reason: Erroneous initiation. Translation N-terminally shortened.The sequence BC007692 differs from that shown. Reason: Erroneous termination at position 428. Translated as Glu.