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KRIT1, Monoclonal Antibody

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產(chǎn)品名稱: KRIT1, Monoclonal Antibody
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KRIT1, Monoclonal Antibody


KRIT1, Monoclonal Antibody  的詳細(xì)介紹
Product Name

KRIT1, Monoclonal Antibody

Full Product Name

KRIT1 (Krev Interaction Trapped Protein 1, Krev Interaction Trapped 1, Cerebral Cavernous Malformations 1 Protein, CCM1)

Product Synonym Names
Anti -KRIT1 (Krev Interaction Trapped Protein 1, Krev Interaction Trapped 1, Cerebral Cavernous Malformations 1 Protein, CCM1)
Product Gene Name

anti-KRIT1 antibody

[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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Immunogen Sequence
AAFFTGQIFT KASPSNHKVI PVYVGVNIKG LHLLNMETKA LLISLKYGCF MWQLGDTDTC FQIHSMENKM SFIVHTKQAG LVVKLLMKLN GQLMPTERNS
Chromosome Location
Chromosome: 7; NC_000007.13 (91828283..91875414, complement). Location: 7q21.2
OMIM
116860
3D Structure
ModBase 3D Structure for O00522
Clonality
Monoclonal
Isotype
IgG2a lambda
Clone Number
2C7
Host
Mouse
Species Reactivity
Human
Specificity
Recognizes human KRIT1.
Purity/Purification
Affinity Purified
Purified by Protein A affinity chromatography.
Form/Format
Supplied as a liquid in PBS, pH 7.2.
Immunogen
Partial recombinant corresponding to aa637-736 from human KRIT1 (NP_004903) with GST tag. MW of the GST tag alone is 26kD.
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 at least 12 months. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
Other Notes
Small volumes of anti-KRIT1 antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
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Related Product Information for
anti-KRIT1 antibody
Component of the CCM signaling pathway which is a crucial regulator of heart and vessel formation and integrity By similarity. Negative regulator of angiogenesis. Inhibits endothelial proliferation, apoptosis, migration, lumen formation and sprouting angiogenesis in primary endothelial cells. Promotes AKT phosphorylation in a NOTCH-dependent and independent manner, and inhibits EKR1/2 phosphorylation indirectly through activation of the DELTA-NOTCH cascade. Acts in concert with CDH5 to establish and maintain correct endothelial cell polarity and vascular lumen and these effects are mediated by recruitment and activation of the Par polarity complex and RAP1B. Required for the localization of phosphorylated PRKCZ, PARD3, TIAM1 and RAP1B to the cell junction, and cell junction stabilization. Plays an important role in the maintenance of the intracellular reactive oxygen species (ROS) homeostasis to prevent oxidative cellular damage. Regulates the homeostasis of intracellular ROS through an antioxidant pathway involving FOXO1 and SOD2. Facilitates the down-regulation of cyclin-D1 (CCND1) levels required for cell transition from proliferative growth to quiescence by preventing the accumulation of intracellular ROS through the modulation of FOXO1 and SOD2 levels.
Product Categories/Family for anti-KRIT1 antibody
Antibodies; Abs to Neuroscience
Applications Tested/Suitable for anti-KRIT1 antibody
ELISA (EL/EIA)
Application Notes for anti-KRIT1 antibody
Suitable for use in ELISA.
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NCBI/Uniprot data below describe general gene information for KRIT1. It may not necessarily be applicable to this product.
NCBI GI #
2149602
NCBI GeneID
889
NCBI Accession #
AAB58582.1 [Other Products]
UniProt Primary Accession #
O00522 [Other Products]
UniProt Secondary Accession #
O43894; Q506L6; Q6U276; Q75N19; Q9H180; Q9H264; Q9HAX5; A6NNU0[Other Products]
UniProt Related Accession #
O00522[Other Products]
Molecular Weight
84,348 Da[Similar Products]
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NCBI Official Full Name
Krit1
NCBI Official Synonym Full Names
KRIT1, ankyrin repeat containing
NCBI Official Symbol
KRIT1??[Similar Products]
NCBI Official Synonym Symbols
CAM; CCM1
??[Similar Products]
NCBI Protein Information
krev interaction trapped protein 1; krev interaction trapped 1; ankyrin repeat-containing protein Krit1; cerebral cavernous malformations 1 protein
UniProt Protein Name
Krev interaction trapped protein 1
UniProt Synonym Protein Names
Cerebral cavernous malformations 1 protein
Protein Family
Krev interaction trapped protein
UniProt Gene Name
KRIT1??[Similar Products]
UniProt Synonym Gene Names
CCM1; Krev interaction trapped 1??[Similar Products]
UniProt Entry Name
KRIT1_HUMAN
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NCBI Summary for KRIT1
This gene encodes a protein containing four ankyrin repeats, a band 4.1/ezrin/radixin/moesin (FERM) domain, and multiple NPXY sequences. The encoded protein is localized in the nucleus and cytoplasm. It binds to integrin cytoplasmic domain-associated protein-1 alpha (ICAP1alpha), and plays a critical role in beta1-integrin-mediated cell proliferation. It associates with junction proteins and RAS-related protein 1A (Rap1A), which requires the encoded protein for maintaining the integrity of endothelial junctions. It is also a microtubule-associated protein and may play a role in microtubule targeting. Mutations in this gene result in cerebral cavernous malformations. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2009]
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UniProt Comments for KRIT1
KRIT1: Component of the CCM signaling pathway which is a crucial regulator of heart and vessel formation and integrity. Negative regulator of angiogenesis. Inhibits endothelial proliferation, apoptosis, migration, lumen formation and sprouting angiogenesis in primary endothelial cells. Promotes AKT phosphorylation in a NOTCH-dependent and independent manner, and inhibits EKR1/2 phosphorylation indirectly through activation of the DELTA-NOTCH cascade. Acts in concert with CDH5 to establish and maintain correct endothelial cell polarity and vascular lumen and these effects are mediated by recruitment and activation of the Par polarity complex and RAP1B. Required for the localization of phosphorylated PRKCZ, PARD3, TIAM1 and RAP1B to the cell junction, and cell junction stabilization. Plays an important role in the maintenance of the intracellular reactive oxygen species (ROS) homeostasis to prevent oxidative cellular damage. Regulates the homeostasis of intracellular ROS through an antioxidant pathway involving FOXO1 and SOD2. Facilitates the down-regulation of cyclin-D1 (CCND1) levels required for cell transition from proliferative growth to quiescence by preventing the accumulation of intracellular ROS through the modulation of FOXO1 and SOD2 levels. Defects in KRIT1 are the cause of cerebral cavernous malformations type 1 (CCM1). Cerebral cavernous malformations (CCMs) are congenital vascular anomalies of the central nervous system that can result in hemorrhagic stroke, seizures, recurrent headaches, and focal neurologic deficits. CCMs have an incidence of 0.1%-0.5% in the general population and usually present clinically during the 3rd to 5th decade of life. The lesions are characterized by grossly enlarged blood vessels consisting of a single layer of endothelium and without any intervening neural tissue, ranging in diameter from a few millimeters to several centimeters. 3 isoforms of the human protein are produced by alternative splicing.

Protein type: Motility/polarity/chemotaxis; G protein regulator, misc.

Chromosomal Location of Human Ortholog: 7q21.2

Cellular Component: extracellular space; microtubule; cytoplasm; plasma membrane; intercellular junction

Molecular Function: protein binding; phosphatidylinositol-4,5-bisphosphate binding; microtubule binding; protein complex binding

Biological Process: negative regulation of angiogenesis; positive regulation of protein binding; regulation of catalytic activity; cell redox homeostasis; small GTPase mediated signal transduction; negative regulation of endothelial cell proliferation; angiogenesis

Disease: Cerebral Cavernous Malformations
Research Articles on KRIT1
1. Genetic testing identified a truncating mutation in the KRIT1 gene in one individual and confirmed the diagnosis of familial cerebral cavernomas as the cause of epilepsy in a family.
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Precautions
All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.
Disclaimer
While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.

It is the responsibility of the customer to report product performance issues to MyBioSource within 30 days of receipt of the product. Please visit our Terms & Conditions page for more information.
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