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Rabbit anti-Human Cleaved-COL1A2 (G1102) Polyclonal Antibody

The antibody against COL1A2 was raised in rabbit using the Synthesized peptide derived from the N-terminal region of Human COL1A2. as the immunogen. This antibody exists as a non-conjugated isotype IgG. The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen. This antibody has been validated on WB, ELISA.

ADC-39939A

The antibody against COL1A2 was raised in rabbit using the Synthesized peptide derived from the N-terminal region of Human COL1A2. as the immunogen. This antibody exists as a non-conjugated isotype IgG. The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen. This antibody has been validated on WB, ELISA.

$167.00

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Specifications


Cat.No ADC-39939A ClonalityPolyclonal
Host SpeciesRabbitTarget NameCOL1A2
FormLiquidSpecies ReactivityHuman
IsotypeIgGStorage Buffer0.5% BSA and 0.02% sodium azide., Liquid in PBS containing 50% glycerol
Purification MethodThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.ConjugateNon-conjugated
ApplicationELISA, WBStorageUpon receipt

Immunogen Information


Immunogen DescriptionSynthesized peptide derived from the N-terminal region of Human COL1A2.Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDP08123
Background Information
  • Uniprot Id

    P08123

  • Target Species

    Human

  • Target Name

    COL1A2

  • Target Full Name

    Collagen alpha-2(I) chain

  • Target Function

    Type I collagen is a member of group I collagen (fibrillar forming collagen).

  • Target Involvement

    Ehlers-Danlos syndrome 7B (EDS7B); Osteogenesis imperfecta 1 (OI1); Osteogenesis imperfecta 2 (OI2); Ehlers-Danlos syndrome, autosomal recessive, cardiac valvular form (EDSCV); Osteogenesis imperfecta 3 (OI3); Osteogenesis imperfecta 4 (OI4)

  • Target Subcellular Location

    Secreted, extracellular space, extracellular matrix.

  • Target Protein Families

    Fibrillar collagen family

  • Target Tissue Specificity

    Forms the fibrils of tendon, ligaments and bones. In bones the fibrils are mineralized with calcium hydroxyapatite.

  • Target Synonyms

    OI4; EDSCV; EDSARTH2; Collagen I/COL1A2

  • Target Background

    This gene encodes the pro-alpha2 chain of type I collagen whose triple helix comprises two alpha1 chains and one alpha2 chain. Type I is a fibril-forming collagen found in most connective tissues and is abundant in bone, cornea, dermis and tendon. Mutations in this gene are associated with osteogenesis imperfecta types I-IV, Ehlers-Danlos syndrome type VIIB, recessive Ehlers-Danlos syndrome Classical type, idiopathic osteoporosis, and atypical Marfan syndrome. Symptoms associated with mutations in this gene, however, tend to be less severe than mutations in the gene for the alpha1 chain of type I collagen (COL1A1) reflecting the different role of alpha2 chains in matrix integrity. Three transcripts, resulting from the use of alternate polyadenylation signals, have been identified for this gene.

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