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Rabbit anti-Human Cyclin D1 Monoclonal Antibody

The antibody against Cyclin D1 was raised in Rabbit using a synthetic peptide corresponding to a sequence within amino acids 196-295 of human Cyclin D1 (P24385) as the immunogen. The monoclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IF/ICC, ELISA.

ADA-17284A

The antibody against Cyclin D1 was raised in Rabbit using a synthetic peptide corresponding to a sequence within amino acids 196-295 of human Cyclin D1 (P24385) as the immunogen. The monoclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IF/ICC, ELISA.

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Specifications


Cat.No ADA-17284A ClonalityMonoclonal
Host SpeciesRabbitTarget NameCyclin D1
Target SynonymsBCL1; PRAD1; U21B31; D11S287E; D1FormLiquid
Species ReactivityHuman, Mouse, RatIsotypeIgG
Storage Buffer50% Glycerol, 0.05% BSA, PBS with 0.02% sodium azide, pH7.3.Purification MethodAffinity purification
Positive SamplesHeLa, HepG2, MCF7, Mouse lungApplicationELISA, WB, IF/ICC

Immunogen Information


Immunogen DescriptionA synthetic peptide corresponding to a sequence within amino acids 196-295 of human Cyclin D1 (P24385).Target SpeciesHuman
Immunogen SequenceISNPPSMVAAGSVVAAVQGLNLRSPNNFLSYYRLTRFLSRVIKCDPDCLRACQEQIEALLESSLRQAQQNMDPKAAEEEEEEEEEVDLACTPTDVRDVDIUniprot IDP24385
Background Information
  • Uniprot Id

    P24385

  • Target Species

    Human

  • Target Name

    CCND1

  • Target Full Name

    G1/S-specific cyclin-D1

  • Target Function

    Regulatory component of the cyclin D1-CDK4 (DC) complex that phosphorylates and inhibits members of the retinoblastoma (RB) protein family including RB1 and regulates the cell-cycle during G(1)/S transition. Phosphorylation of RB1 allows dissociation of the transcription factor E2F from the RB/E2F complex and the subsequent transcription of E2F target genes which are responsible for the progression through the G(1) phase. Hypophosphorylates RB1 in early G(1) phase. Cyclin D-CDK4 complexes are major integrators of various mitogenenic and antimitogenic signals. Also substrate for SMAD3, phosphorylating SMAD3 in a cell-cycle-dependent manner and repressing its transcriptional activity. Component of the ternary complex, cyclin D1/CDK4/CDKN1B, required for nuclear translocation and activity of the cyclin D-CDK4 complex. Exhibits transcriptional corepressor activity with INSM1 on the NEUROD1 and INS promoters in a cell cycle-independent manner.

  • Target Involvement

    Multiple myeloma (MM)

  • Target Subcellular Location

    Nucleus. Cytoplasm. Nucleus membrane.

  • Target Protein Families

    Cyclin family, Cyclin D subfamily

  • Target Research Area

    Cell Cycle

  • Target Synonyms

    AI327039; B cell CLL/lymphoma 1; B cell leukemia 1; B cell lymphoma 1 protein; B-cell lymphoma 1 protein; BCL 1; BCL-1; BCL-1 oncogene; BCL1; BCL1 oncogene; ccnd1; CCND1/FSTL3 fusion gene; CCND1/FSTL3 fusion gene; included; CCND1/IGHG1 fusion gene; CCND1/IGHG1 fusion gene; included; CCND1/IGLC1 fusion gene; CCND1/IGLC1 fusion gene; included; CCND1/PTH fusion gene; CCND1/PTH fusion gene; included; CCND1_HUMAN; cD1; Cyl 1; D11S287E; G1/S specific cyclin D1; G1/S-specific cyclin-D1; Parathyroid adenomatosis 1; PRAD1; PRAD1 oncogene; U21B31

  • Target Background

    The protein encoded by this gene belongs to the highly conserved cyclin family, whose members are characterized by a dramatic periodicity in protein abundance throughout the cell cycle. Cyclins function as regulators of CDK kinases. Different cyclins exhibit distinct expression and degradation patterns which contribute to the temporal coordination of each mitotic event. This cyclin forms a complex with and functions as a regulatory subunit of CDK4 or CDK6, whose activity is required for cell cycle G1/S transition. This protein has been shown to interact with tumor suppressor protein Rb and the expression of this gene is regulated positively by Rb. Mutations, amplification and overexpression of this gene, which alters cell cycle progression, are observed frequently in a variety of human cancers.

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