Rabbit Polyclonal VCP antibody (STJ96231)

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Reactivity: Human, Mouse, Rat
Applications: WB, IHC, ELISA
Conjugation: Unconjugated
Supplier: St John’s Laboratory Ltd.

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Rabbit Polyclonal VCP antibody (STJ96231)

Supplier: St John’s Laboratory Ltd.

Recommended applications: WB, IHC, ELISA

Recommended dilution: WB 1:500-1:2000; IHC 1:100-1:300; ELISA 1:40000;

Recommended protocols: check protocols

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Alternative names:

Check alternative names for the antibody

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VCP antibody,|15S Mg(2+) ATPase p97 subunit antibody|15S Mg(2+)-ATPase p97 subunit antibody|ALS14 antibody|ATPase p97 antibody|CDC48 antibody|IBMPFD antibody|MGC131997 antibody|MGC148092 antibody|MGC8560 antibody|p97 antibody|TER ATPase antibody|TERA antibody|TERA_HUMAN antibody|Transitional endoplasmic reticulum ATPase antibody|Valosin containing protein antibody|Valosin-containing protein antibody|VCP antibody|Yeast Cdc48p homolog antibody|Anti-VCP antibody [5] (ab11433)
SCBT cat No: To be updated

 

Name

VCP Polyclonal Antibody

Catalogue No.

STJ96231

Reactivity

Human, Mouse, Rat

Specificity

VCP Polyclonal Antibody detects endogenous levels of VCP protein.

Immunogen

Synthesized peptide derived from VCP at AA range 290-370

Host

Rabbit

Applications

WB, IHC, ELISA

Recommended dilution

WB 1:500-1:2000; IHC 1:100-1:300; ELISA 1:40000;

Clonality

Polyclonal

Conjugation

Unconjugated

Isotype

IgG

Molecular weight

85 kDa

Formulation

VCP Antibody was tube-contained. Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

Concentration

1 mg/ml

Purification

VCP Antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Storage

-20 Celsius degree. Avoid repeated freeze/thaw cycles.

Alternative antibody names

Transitional endoplasmic reticulum ATPase antibody, TER ATPase antibody, 15S Mgantibody, 2+ antibody,-ATPase p97 subunit antibody, Valosin-containing protein antibody, VCP antibody

Database links

Human UniProt/Swiss-Prot:P55072;Mouse UniPort/Swiss-Prot: Q01853;Rat UniProt/Swiss-Port: P46462;Human Entrez Gene: 7415;Mouse Entrez Gene: 269523;Rat Entrez Gene: Rn.98891

Protein names

Transitional endoplasmic reticulum ATPase , TER ATPase , 15S Mg, 2+ ,-ATPase p97 subunit , Valosin-containing protein , VCP

Protein function

Necessary for the fragmentation of Golgi stacks during mitosis and for their reassembly after mitosis. Involved in the formation of the transitional endoplasmic reticulum (tER). The transfer of membranes from the endoplasmic reticulum to the Golgi apparatus occurs via 50-70 nm transition vesicles which derive from part-rough, part-smooth transitional elements of the endoplasmic reticulum (tER). Vesicle budding from the tER is an ATP-dependent process. The ternary complex containing UFD1L, VCP and NPLOC4 binds ubiquitinated proteins and is necessary for the export of misfolded proteins from the ER to the cytoplasm, where they are degraded by the proteasome. The NPLOC4-UFD1L-VCP complex regulates spindle disassembly at the end of mitosis and is necessary for the formation of a closed nuclear envelope. Regulates E3 ubiquitin-protein ligase activity of RNF19A. Component of the VCP/p97-AMFR/gp78 complex that participates in the final step of the sterol-mediated ubiquitination and endoplasmic reticulum-associated degradation (ERAD) of HMGCR. Also involved in DNA damage response: recruited to double-strand breaks (DSBs) sites in a RNF8- and RNF168-dependent manner and promotes the recruitment of TP53BP1 at DNA damage sites. Recruited to stalled replication forks by SPRTN: may act by mediating extraction of DNA polymerase eta (POLH) to prevent excessive translesion DNA synthesis and limit the incidence of mutations induced by DNA damage. Required for cytoplasmic retrotranslocation of stressed/damaged mitochondrial outer-membrane proteins and their subsequent proteasomal degradation. / ATP + H2O = ADP + phosphate.

Involvement in disease

Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1 (IBMPFD1) [MIM:167320]: An autosomal dominant disease characterized by disabling muscle weakness clinically resembling to limb girdle muscular dystrophy, osteolytic bone lesions consistent with Paget disease, and premature frontotemporal dementia. Clinical features show incomplete penetrance. . Note: The disease is caused by mutations affecting the gene represented in this entry.; Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia (ALS14) [MIM:613954]: A neurodegenerative disorder affecting upper motor neurons in the brain and lower motor neurons in the brain stem and spinal cord, resulting in fatal paralysis. Sensory abnormalities are absent. The pathologic hallmarks of the disease include pallor of the corticospinal tract due to loss of motor neurons, presence of ubiquitin-positive inclusions within surviving motor neurons, and deposition of pathologic aggregates. The etiology of amyotrophic lateral sclerosis is likely to be multifactorial, involving both genetic and environmental factors. The disease is inherited in 5-10% of the cases. Patients with ALS14 may develop frontotemporal dementia. . Note: The disease is caused by mutations affecting the gene represented in this entry.; Charcot-Marie-Tooth disease 2Y (CMT2Y) [MIM:616687]: An autosomal dominant, axonal form of Charcot-Marie-Tooth disease, a disorder of the peripheral nervous system, characterized by progressive weakness and atrophy, initially of the peroneal muscles and later of the distal muscles of the arms. Charcot-Marie-Tooth disease is classified in two main groups on the basis of electrophysiologic properties and histopathology: primary peripheral demyelinating neuropathies (designated CMT1 when they are dominantly inherited) and primary peripheral axonal neuropathies (CMT2). Neuropathies of the CMT2 group are characterized by signs of axonal degeneration in the absence of obvious myelin alterations, normal or slightly reduced nerve conduction velocities, and progressive distal muscle weakness and atrophy. . Note: The disease is caused by mutations affecting the gene represented in this entry.

Protein sequence and domain

Belongs to the AAA ATPase family.

Protein post-translational modifications

Phosphorylated by tyrosine kinases in response to T-cell antigen receptor activation. / ISGylated. / Methylation at Lys-315 catalyzed by VCPKMT is increased in the presence of ASPSCR1. Lys-315 methylation may decrease ATPase activity.

Protein cellular localization

Cytoplasm > cytosol / Endoplasmic reticulum / Nucleus

Research area

All research areas>Cell Cycle Proteins>VCP
(View all antibody categories related to Cell Cycle Proteins)

Note

AntibodyPlus can customize VCP Antibody according to your requirement, including bulk product size,etc. Please contact info@antibodyplus.com. AntibodyPlus provide antibody trial sample for your own antibody validation and collects antibody reviews.

Supplier

St John’s Laboratory Ltd.

Product type

Primary antibody

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Antibody customer reviews & validation data - 11

Validation data ID: 11

Submission date: 2016-11-18

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Result figure:
Result figure

Figure description:

Two separate lanes have shown identical result using VCP antibody, indicating a good reproducibility.

Product name

rabbit polyclonal VCP antibody

Product catalog No.

STJ96231

Product type

Primary antibody

Supplier

St John's Laboratory Ltd

Application type

Western Blot

Antibody specificity rating

Good

Antibody overall rating

Good

Your comments

We are very satisfied with all the trial antibodies!

Detailed protocol

View Details

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Antibody customer reviews & validation data - 11

Validation data ID: 11

Submission date: 2016-11-18

View Details

Result figure:
Result figure

Figure description:

Two separate lanes have shown identical result using VCP antibody, indicating a good reproducibility.

Product name

rabbit polyclonal VCP antibody

Product catalog No.

STJ96231

Product type

Primary antibody

Supplier

St John's Laboratory Ltd

Application type

Western Blot

Antibody specificity rating

Good

Antibody overall rating

Good

Your comments

We are very satisfied with all the trial antibodies!

Detailed protocol

View Details

view database submit reviews

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