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Thermo Fisher Scientific GALE Polyclonal Antibody
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Thermo Fisher Scientific GALE Polyclonal Antibody

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Rabbit polyclonal antibody targeting human GALE protein. Validated for ICC/IF applications with high specificity. Supplied as a liquid, unconjugated form at 0.2 mg/mL. Suitable for research use only, not for diagnostic procedures.

카탈로그번호
PA5144982
판매단위
pk
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마지막 업데이트 2025. 07. 22. 오후 09:36
Thermo Fisher Scientific PA5144982 GALE Polyclonal Antibody 100 ul pk판매 단위 pk
재고 1개
890,600원VAT 포함 979,660원

Thermo Fisher Scientific · Thermo Fisher Scientific GALE Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Immunocytochemistry (ICC/IF) 0.25–2 µg/mL

Product Specifications

Specification Description
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant Protein Epitope Signature Tag (PrEST) antigen sequence, range 58–182. Recombinant protein control fragment (Product # RP-109862)
Conjugate Unconjugated
Form Liquid
Concentration 0.2 mg/mL
Purification Affinity chromatography
Storage Buffer PBS, pH 7.2, with 40% glycerol
Contains 0.02% 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_3091802

Product Specific Information

Immunogen sequence:

RSVEFEEMDI LDQGALQRLF KKYSFMAVIH FAGLKAVGES VQKPLDYYRV NLTGTIQLLE IMKAHGVKNL VFSSSATVYG NPQYLPLDEA HPTGGCTNPY GKSKFFIEEM IRDLCQADKT WNAVL

Antigen sequence identity:
Mouse 94%; Rat 91%


Target Information

This gene encodes UDP-galactose-4-epimerase, an enzyme catalyzing two analogous reactions:

  • Epimerization of UDP-glucose to UDP-galactose
  • Epimerization of UDP-N-acetylglucosamine to UDP-N-acetylgalactosamine

The enzyme’s bifunctional nature means mutant cells or individuals rely on exogenous galactose and N-acetylgalactosamine for glycoprotein and glycolipid synthesis.
Mutations in this gene cause epimerase-deficiency galactosemia (galactosemia type 3), characterized by liver damage, early-onset cataracts, deafness, and mental retardation, with severity ranging from mild (peripheral form) to severe (generalized form).
Multiple alternatively spliced transcripts encoding the same protein have been identified.


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

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