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ABL1 antibody (pTyr412)

The Rabbit Polyclonal anti-ABL1 antibody has been validated for WB and IHC. It is suitable to detect ABL1 in samples from Human.
Catalog No. ABIN7265966

Quick Overview for ABL1 antibody (pTyr412) (ABIN7265966)

Target

See all ABL1 Antibodies
ABL1 (C-Abl Oncogene 1, Non-Receptor tyrosine Kinase (ABL1))

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This ABL1 antibody is un-conjugated

Application

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Western Blotting (WB), Immunohistochemistry (IHC)
  • Binding Specificity

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    pTyr412

    Purpose

    Phospho-ABL1-Y412 Rabbit pAb

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Phosphorylated Antibodies

    Purification

    Affinity purification

    Immunogen

    A phospho synthetic peptide corresponding to residues surrounding Y412 of human ABL1.

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IHC,1:50 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    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

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    ABL1 (C-Abl Oncogene 1, Non-Receptor tyrosine Kinase (ABL1))

    Alternative Name

    ABL1

    Background

    This gene is a protooncogene that encodes a protein tyrosine kinase involved in a variety of cellular processes, including cell division, adhesion, differentiation, and response to stress. The activity of the protein is negatively regulated by its SH3 domain, whereby deletion of the region encoding this domain results in an oncogene. The ubiquitously expressed protein has DNA-binding activity that is regulated by CDC2-mediated phosphorylation, suggesting a cell cycle function. This gene has been found fused to a variety of translocation partner genes in various leukemias, most notably the t(9,22) translocation that results in a fusion with the 5' end of the breakpoint cluster region gene (BCR, MIM:151410). Alternative splicing of this gene results in two transcript variants, which contain alternative first exons that are spliced to the remaining common exons.,ABL,JTK7,p150,c-ABL,v-abl,CHDSKM,c-ABL1,ABL1,c-Abl,bcr/abl,Apoptosis,Cancer,Cell Biology & Developmental Biology,Cell Cycle,Cytoskeleton_Microtubules,Epigenetics & Nuclear Signaling,ErbB-HER Signaling Pathway,G1/S Checkpoint,G2/M DNA Damage Checkpoint,Immunology & Inflammation,Kinase,Kinase_Tyrosine kinases,MAPK-JNK Signaling Pathway,Protein phosphorylation,Signal Transduction,TGF-b-Smad Signaling Pathway,ABL1

    Molecular Weight

    123kDa

    Gene ID

    25

    UniProt

    P00519

    Pathways

    Apoptosis, Regulation of Muscle Cell Differentiation, Platelet-derived growth Factor Receptor Signaling, Lipid Metabolism
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