• Western blot testing of human 1) placenta, 2) T-47D, 3) U-2 OS, 4) K562, 5) ThP-1 and 6) monkey COS-7 lysate with CPAMD8 antibody at 0.5ug/ml. Predicted molecular weight ~207 kDa.
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NSJ Bioreagents

RQ4937

CPAMD8 Antibody

CPAMD8 Antibody

$449.00 USD
$449.00 USD
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CPAMD8 belongs to the complement component-3 (C3) / alpha-2-macroglobulin (A2M) family of proteins, which are involved in innate immunity and damage control. The encoded protein is membrane-associated and proteolytically processed to generate two chains. Mutations in this gene cause a form of anterior segment dysgenesis, a developmental disorder of the eye. By genomic sequence analysis, the CPAMD8 gene is mapped to chromosome 19p13.3-p13.2.

Specifications

Family Primary antibody
Formulation 0.5mg/ml if reconstituted with 0.2ml sterile DI water
Format Antigen affinity purified
Host Animal Rabbit
Clonality Polyclonal (rabbit origin)
Isotype Rabbit IgG
Species Reactivity Human, Monkey
Application WB, IHC-P, Direct ELISA
Application Details Western blot: 0.5-1ug/ml, Immunohistochemistry (FFPE): 1-2ug/ml, Direct ELISA: 0.1-0.5ug/ml
Application Note Optimal dilution of the CPAMD8 antibody should be determined by the researcher.
Localization Cytoplasmic
Immunogen Amino acids R58-D234 from the human protein were used as the immunogen for the CPAMD8 antibody.
Buffer Lyophilized from 1X PBS with 2% Trehalose and 0.025% sodium azide
Purity Antigen affinity purified
Storage After reconstitution, the CPAMD8 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
Limitation This CPAMD8 antibody is available for research use only.
Uniprot # Q8IZJ3
Status Available
PDF Link https://www.nsjbio.com/tds-pdf/cpamd8-antibody-rq4937
Title CPAMD8 Antibody
Description CPAMD8 belongs to the complement component-3 (C3) / alpha-2-macroglobulin (A2M) family of proteins, which are involved in innate immunity and damage control. The encoded protein is membrane-associated and proteolytically processed to generate two chains. Mutations in this gene cause a form of anterior segment dysgenesis, a developmental disorder of the eye. By genomic sequence analysis, the CPAMD8 gene is mapped to chromosome 19p13.3-p13.2.
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