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Rabbit anti-Human TPM2 Polyclonal Antibody

The antibody against TPM2 was raised in Rabbit using a synthetic peptide corresponding to a sequence within amino acids 1-100 of human TPM2 (NP_003280.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IHC-P, IF/ICC, IP, ELISA.

ADA-04183A

The antibody against TPM2 was raised in Rabbit using a synthetic peptide corresponding to a sequence within amino acids 1-100 of human TPM2 (NP_003280.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IHC-P, IF/ICC, IP, ELISA.

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Specifications


Cat.No ADA-04183A ClonalityPolyclonal
Host SpeciesRabbitTarget NameTPM2
Target SynonymsDA1; DA2B; NEM4; TMSB; AMCD1; DA2B4; HEL-S-273; TPM2FormLiquid
Species ReactivityHuman, Mouse, RatIsotypeIgG
Storage Buffer50% Glycerol, PBS with 0.01% thimerosal, pH7.3.Purification MethodAffinity purification
Positive SamplesHeLa, MCF7, Mouse lung, Mouse skeletal muscle, SW620, U-87MGApplicationELISA, WB, IF/ICC, IHC-P, IP

Immunogen Information


Immunogen DescriptionA synthetic peptide corresponding to a sequence within amino acids 1-100 of human TPM2 (NP_003280.2).Target SpeciesHuman
Immunogen SequenceMDAIKKKMQMLKLDKENAIDRAEQAEADKKQAEDRCKQLEEEQQALQKKLKGTEDEVEKYSESVKEAQEKLEQAEKKATDAEADVASLNRRIQLVEEELDUniprot IDP07951
Background Information
  • Uniprot Id

    P07951

  • Target Species

    Human

  • Target Name

    TPM2

  • Target Full Name

    Tropomyosin beta chain

  • Target Function

    Binds to actin filaments in muscle and non-muscle cells. Plays a central role, in association with the troponin complex, in the calcium dependent regulation of vertebrate striated muscle contraction. Smooth muscle contraction is regulated by interaction with caldesmon. In non-muscle cells is implicated in stabilizing cytoskeleton actin filaments. The non-muscle isoform may have a role in agonist-mediated receptor internalization.

  • Target Involvement

    Nemaline myopathy 4 (NEM4); Arthrogryposis, distal, 1A (DA1A); Cap myopathy 2 (CAPM2); Arthrogryposis, distal, 2B (DA2B)

  • Target Subcellular Location

    Cytoplasm, cytoskeleton.

  • Target Protein Families

    Tropomyosin family

  • Target Tissue Specificity

    Present in primary breast cancer tissue, absent from normal breast tissue.

  • Target Research Area

    Signal Transduction

  • Target Synonyms

    Alpha tropomyosin; AMCD1; Arthrogryposis multiplex congenital distal type 1; Beta tropomyosin; Beta-tropomyosin; Cytoskeletal tropomyosin TM30; DA1; DA2B; epididymis secretory protein Li 273; FLJ41118; Heat stable cytoskeletal protein 30 kDa; HEL-S-273; hscp30; HTM alpha; hTM5; MGC14582; MGC3261; MGC72094; NEM1; NEM4; Nemaline myopathy type 4; OK/SW cl.5; Sarcomeric tropomyosin kappa; TM 5; TM3; TM30; TM30nm; TMSA; TMSB; TPM 1; TPM 3; TPM1 alpha; TPM1 kappa; TPM2; TPM2_HUMAN; TRK; Tropomyosin 1 alpha; Tropomyosin 1 alpha chain; Tropomyosin 1 alpha chain isoform 6; Tropomyosin 2 (beta); Tropomyosin 2; Tropomyosin 3; Tropomyosin alpha 3 chain; Tropomyosin alpha striated muscle isoform; Tropomyosin beta chain; Tropomyosin gamma; Tropomyosin skeletal muscle beta; Tropomyosin-2

  • Target Background

    This gene encodes beta-tropomyosin, a member of the actin filament binding protein family, and mainly expressed in slow, type 1 muscle fibers. Mutations in this gene can alter the expression of other sarcomeric tropomyosin proteins, and cause cap disease, nemaline myopathy and distal arthrogryposis syndromes. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

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