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KRIT1 antibody (C-Term)

This anti-KRIT1 antibody is a Rabbit Polyclonal antibody detecting KRIT1 in WB. Suitable for Human, Mouse and Rat.
Catalog No. ABIN4886652

Quick Overview for KRIT1 antibody (C-Term) (ABIN4886652)

Target

See all KRIT1 Antibodies
KRIT1 (KRIT1, Ankyrin Repeat Containing (KRIT1))

Reactivity

Human, Mouse, Rat

Host

  • 35
  • 4
Rabbit

Clonality

  • 35
  • 4
Polyclonal

Conjugate

  • 16
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This KRIT1 antibody is un-conjugated

Application

  • 32
  • 17
  • 13
  • 13
  • 4
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 15
    • 6
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 703-736, C-Term

    Purpose

    Anti-KRIT1 Antibody Picoband®

    Sequence

    ENKMSFIVHT KQAGLVVKLL MKLNGQLMPT ERNS

    Cross-Reactivity (Details)

    No cross-reactivity with other proteins.

    Characteristics

    Anti-KRIT1 Antibody Picoband® (ABIN4886652). Tested in WB applications. This antibody reacts with Human, Mouse, Rat. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.

    Purification

    Immunogen affinity purified.

    Immunogen

    A synthetic peptide corresponding to a sequence at the C-terminus of human KRIT1, different from the related mouse sequence by one amino acid.

    Isotype

    IgG
  • Application Notes

    Western blot, 0.1-0.5 μg/mL, Human, Mouse, Rat
    1. Eerola I, McIntyre B, Vikkula M (Feb 2001). "Identification of eight novel 5'-exons in cerebral capillary malformation gene-1 (CCM1) encoding KRIT1".Biochimica et Biophysica Acta 1517 (3): 464-7. 2. Pagenstecher A, Stahl S, Sure U, Felbor U (Mar 2009)."A two-hit mechanism causes cerebral cavernous malformations: complete inactivation of CCM1, CCM2 or CCM3 in affected endothelial cells". Human Molecular Genetics 18 (5): 911-8.

    Comment

    Antibody can be supported by chemiluminescence kit ABIN921124 in WB.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    Concentration

    500 μg/mL

    Buffer

    Each vial contains 5 mg BSA, 0.9 mg NaCl, 0.2 mg Na2HPO4, 0.05 mg 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.

    Handling Advice

    Avoid repeated freezing and thawing.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store at -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freeze-thaw cycles.
  • Target

    KRIT1 (KRIT1, Ankyrin Repeat Containing (KRIT1))

    Alternative Name

    KRIT1

    Background

    Synonyms: Krev interaction trapped protein 1,Krev interaction trapped 1,Cerebral cavernous malformations 1 protein,KRIT1,CCM1,

    Tissue Specificity: Low levels in brain. Very weak expression found in heart and muscle. .

    Background: Krev interaction trapped protein 1 (KRIT1) is a protein that in humans is encoded by the CCM1 gene. 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.

    Molecular Weight

    84 kDa

    Gene ID

    889

    UniProt

    O00522

    Pathways

    Cell RedoxHomeostasis
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