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Thermo Fisher Scientific GBA Recombinant Rabbit Monoclonal Antibody (JM10-76)
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Thermo Fisher Scientific GBA Recombinant Rabbit Monoclonal Antibody (JM10-76)

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Recombinant rabbit monoclonal antibody targeting human GBA protein. Validated for WB and IHC applications. Offers high specificity, consistency, and animal-free formulation. Supplied in liquid form with 1 mg/mL concentration and stored at 4°C or -20°C.

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마지막 업데이트 2025. 08. 05. 오전 01:01
Thermo Fisher Scientific MA532591 GBA Recombinant Rabbit Monoclonal Antibody (JM10-76) 100 ul pk판매 단위 pk ·
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622,700원VAT 포함 684,970원

Thermo Fisher Scientific · Thermo Fisher Scientific GBA Recombinant Rabbit Monoclonal Antibody (JM10-76)

Applications

Application Tested Dilution
Western Blot (WB) 1:2,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:500

Product Specifications

Property Description
Species Reactivity Human, Rat
Host / Isotype Rabbit / IgG
Expression System HEK293 cells
Class Recombinant Monoclonal
Type Antibody
Clone JM10-76
Immunogen Synthetic peptide within Human GBA (aa 477–534)
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein A
Storage Buffer TBS, pH 7.4, with 40% Glycerol, 0.05% BSA
Contains 0.05% sodium azide
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_2809868

Product Specific Information

Recombinant rabbit monoclonal antibodies are produced using in vitro expression systems. The antibody DNA sequences from immunoreactive rabbits are cloned and expressed, followed by clone screening to identify optimal candidates.
These antibodies provide:

  • Enhanced specificity and sensitivity
  • Lot-to-lot consistency
  • Animal origin-free formulations
  • Broader immunoreactivity due to the large rabbit immune repertoire

Target Information

Gene: GBA
GBA encodes a lysosomal membrane protein that cleaves the beta-glucosidic linkage of glycosylceramide, an intermediate in glycolipid metabolism.
Mutations in this gene cause Gaucher disease, a lysosomal storage disorder characterized by the accumulation of glucocerebrosides.
A related pseudogene is located approximately 12 kb downstream on chromosome 1. Alternative splicing produces multiple transcript variants.


For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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