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Thermo Fisher Scientific GNAS Polyclonal Antibody
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Thermo Fisher Scientific GNAS Polyclonal Antibody

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GNAS 단백질을 인식하는 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody. Western blot 및 IHC(P) 검증 완료. 다양한 종에서 높은 예측 반응성. 고농축 액상 형태로 제공되며, 장기 보관 시 -20°C에서 보관 권장.

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마지막 업데이트 2025. 07. 30. 오후 12:56
Thermo Fisher Scientific PA521702 GNAS Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
601,500원VAT 포함 661,650원

Thermo Fisher Scientific · Thermo Fisher Scientific GNAS Polyclonal Antibody

Applications

Western Blot (WB)

  • Tested Dilution: 1:500–1:3,000

Immunohistochemistry (Paraffin) (IHC (P))

  • Tested Dilution: 1:100–1:1,000

Product Specifications

항목 내용
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant fragment corresponding to amino acids 716–998 of GNAS (Uniprot ID#Q5JWF2)
Conjugate Unconjugated
Form Liquid
Concentration 0.78 mg/mL
Storage Conditions Store at 4°C short term. For long term, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_11153178

Product Specific Information

  • Recommended positive controls: A431, Mouse brain
  • Predicted reactivity: Mouse (99%), Rat (99%), Xenopus laevis (91%), Xenopus tropicalis (90%), Dog (100%), Pig (100%), Bovine (99%)
  • Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.

Target Information

Mutations in the GNAS gene result in pseudohypoparathyroidism type 1a and 1b, Albright hereditary osteodystrophy, pseudopseudohypoparathyroidism, McCune-Albright syndrome, progressive osseous heteroplasia, polyostotic fibrous dysplasia of bone, and certain pituitary tumors.
This gene exhibits complex imprinted expression patterns, encoding maternally, paternally, and biallelically expressed proteins derived from alternatively spliced transcripts. Each upstream exon resides within a differentially methylated region, typical of imprinted genes. The close proximity (14 kb) of two oppositely expressed promoter regions is unusual.
One alternate 5' exon introduces a frameshift, producing an isoform structurally unrelated to others. An antisense transcript may regulate imprinting in this region. Mutations cause pseudohypoparathyroidism type 1a (PHP1a), which shows atypical autosomal dominant inheritance requiring maternal transmission for full penetrance.

Safety Information

WARNING: This product can expose you to chemicals including mercury, which is known to the State of California to cause birth defects or other reproductive harm.
For more information, visit www.P65Warnings.ca.gov.

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

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