Glypican 3 antibody
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- Target See all Glypican 3 (GPC3) Antibodies
- Glypican 3 (GPC3)
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Monoclonal
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Conjugate
- This Glypican 3 antibody is un-conjugated
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Application
- Immunofluorescence (IF), Western Blotting (WB), Flow Cytometry (FACS), Immunocytochemistry (ICC)
- Cross-Reactivity
- Human
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human Glypican 3
- Clone
- G8A2
- Isotype
- IgG
- Top Product
- Discover our top product GPC3 Primary Antibody
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- Application Notes
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WB 1:300-5000
FCM 1:20-100
IF()
ICC 1:100-500 - Restrictions
- For Research Use only
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- Concentration
- 1 mg/mL
- Buffer
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
- Preservative
- ProClin
- Precaution of Use
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Storage
- 4 °C,-20 °C
- Storage Comment
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- Expiry Date
- 12 months
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- Target
- Glypican 3 (GPC3)
- Alternative Name
- Glypican 3 (GPC3 Products)
- Synonyms
- GPC3 antibody, sgb antibody, dgsx antibody, sdys antibody, sgbs antibody, oci-5 antibody, sgbs1 antibody, DGSX antibody, GTR2-2 antibody, MXR7 antibody, OCI-5 antibody, SDYS antibody, SGB antibody, SGBS antibody, SGBS1 antibody, Glypican-3 antibody, glypican 3 antibody, gpc3 antibody, GPC3 antibody, Gpc3 antibody
- Background
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Synonyms: GPC3, glypican3, glypican-3, Intestinal protein OCI-5, GTR2-2, MXR7.Intestinal protein OCI-5, GPC3_HUMAN.
Background: Cell surface heparan sulfate proteoglycans are composed of a membrane-associated protein core substituted with a variable number of heparan sulfate chains. Members of the glypican-related integral membrane proteoglycan family (GRIPS) contain a core protein anchored to the cytoplasmic membrane via a glycosyl phosphatidylinositol linkage. These proteins may play a role in the control of cell division and growth regulation. The protein encoded by this gene can bind to and inhibit the dipeptidyl peptidase activity of CD26, and it can induce apoptosis in certain cell types. Deletion mutations in this gene are associated with Simpson-Golabi-Behmel syndrome, also known as Simpson dysmorphia syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]
- Gene ID
- 2719
- UniProt
- P51654
- Pathways
- Glycosaminoglycan Metabolic Process
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