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Work with LifeSpan to design a custom immunohistochemistry to address your specific biological question. Outsource the entire localization process without having to worry about finding and characterizing target specific antibodies, sourcing and validating difficult-to-find tissues, and having the ability to interpret the resulting immunostaining in relation to complex human pathologies.

Test your therapeutic antibodies in immunohistochemistry against a broad panel of normal frozen human tissue types in order to determine potential unintended binding. Our non-GLP TCR services are designed on the FDA recommendation outlined in their "Points to Consider in the Manufacture and Testing of Monoclonal Antibody Products for Human Use".

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GALC / Galactocerebrosidase Antibody (PE) LS‑C650375
Galactocerebrosidase antibody LS-C650375 is a PE-conjugated rabbit polyclonal antibody to human Galactocerebrosidase (GALC). Validated for WB.
Antibody
Catalog
Size
Price
LS-C650375-100
100 µl
$755

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Antibody
Species: Human
Applications: IHC, Western blot, ELISA
Antibody
Species: Human
Applications: IHC, Western blot, ELISA

Product Description

Galactocerebrosidase antibody LS-C650375 is a PE-conjugated rabbit polyclonal antibody to human Galactocerebrosidase (GALC). Validated for WB.

Specifications

Target
Human GALC / Galactocerebrosidase
Synonyms
GALC, Galactocerebrosidase, GALCERase, Galactosylceramidase, Galactosylceraminidase
Host
Rabbit
Reactivity
Human (tested or 100% immunogen sequence identity)
Clonality
IgG Polyclonal
Conjugations
Phycoerythrin. Also available Unconjugated or conjugated with AP, APC, Biotin, FITC, HRP.
Purification
Protein A purified
Modifications
Unmodified
Applications
  • Western blot
  • (applications tested for the base form of this product only)
Immunogen
Full length human GALC, aa1-669 (AAH36518.1).
Specificity
Human GALC / Galactocerebrosidase
Presentation
PBS, pH 7.2, No preservatives added
Storage
Store at 4°C. Do not freeze.
Restrictions
For research use only.
About GALC / Galactocerebrosidase
Galactocerebrosidase (GALC) is a lysosomal enzyme that hydrolyzes several galactolipids. GALC deficiency is associated with Krabbe disease (globoid cell leukodystrophy). The gene is about 60 kb in length and consists of 17 exons. This gene contains ten GC-box-like sequences within the promoter region but no typical TATA box. This feature is also characteristic of other lysosomal protein encoding genes. P54803 NM_000153 NP_000144.2


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Requested From: United States
Date Requested: 11/15/2018

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