PRELP antibody (AA 69-353)
Quick Overview for PRELP antibody (AA 69-353) (ABIN7602298)
Target
See all PRELP AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 69-353
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Purpose
- Anti-PRELP Antibody
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Cross-Reactivity (Details)
- No cross-reactivity with other proteins.
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Characteristics
- Anti-PRELP Antibody (ABIN7602298). Tested in ELISA, WB, Flow Cytometry applications. This antibody reacts with Human, Mouse, Rat. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications.
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Purification
- Immunogen affinity purified.
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Immunogen
- E.coli-derived human PRELP recombinant protein (Position: I69-R353).
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Isotype
- IgG
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Application Notes
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Western blot, 0.1-0.25 μg/mL, Human, Mouse, Rat
Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
ELISA, 0.1-0.5 μg/mL, -
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
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Concentration
- 500 μg/mL
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Buffer
- Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.
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Storage
- 4 °C,-20 °C
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Storage Comment
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At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
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- PRELP (Proline Arginine Rich End Leucine Rich Repeat Protein (PRELP))
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Alternative Name
- PRELP
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Background
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Synonyms: Cadherin-4, Retinal cadherin, R-CAD, R-cadherin, CDH4
Tissue Specificity: Expressed mainly in brain but also found in other tissues.
Background: Prolargin is a protein that in humans is encoded by the PRELP gene. The protein encoded by this gene is a leucine-rich repeat protein present in connective tissue extracellular matrix. This protein functions as a molecule anchoring basement membranes to the underlying connective tissue. This protein has been shown to bind type I collagen to basement membranes and type II collagen to cartilage. It also binds the basement membrane heparan sulfate proteoglycan perlecan. This protein is suggested to be involved in the pathogenesis of Hutchinson-Gilford progeria (HGP), which is reported to lack the binding of collagen in basement membranes and cartilage. Alternatively spliced transcript variants encoding the same protein have been observed.
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Molecular Weight
- 65 kDa
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Gene ID
- 5549
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UniProt
- P51888
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Pathways
- Glycosaminoglycan Metabolic Process
Target
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