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Thermo Fisher Scientific GNAS Monoclonal Antibody (OTI13G5), TrueMAB
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Thermo Fisher Scientific GNAS Monoclonal Antibody (OTI13G5), TrueMAB

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GNAS 단백질을 인식하는 Mouse IgG2a 단클론 항체로, Western blot 및 IHC(P)에서 검증됨. 인간 시료에 반응하며, 동결건조 형태로 제공. 재구성 및 결합 실험용으로 적합하며, 연구용으로만 사용 가능.

카탈로그번호
CF809325
판매단위
pk
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마지막 업데이트 2025. 08. 03. 오전 09:07
Thermo Fisher Scientific CF809325 GNAS Monoclonal Antibody (OTI13G5), TrueMAB 100 ug pk판매 단위 pk ·
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784,000원VAT 포함 862,400원

Thermo Fisher Scientific · Thermo Fisher Scientific GNAS Monoclonal Antibody (OTI13G5), TrueMAB

Applications

Western Blot (WB)

  • Tested Dilution: 1:500–1:2,000

Immunohistochemistry (Paraffin) (IHC (P))

  • Tested Dilution: 1:2,000

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG2a
Class Monoclonal
Type Antibody
Clone OTI13G5
Immunogen Full length human recombinant protein of human GNAS produced in HEK293T Cell
Conjugate Unconjugated
Form Lyophilized
Concentration 1 mg/mL
Purification Affinity chromatography
Storage Buffer PBS, pH 7.3, with 8% trehalose
Contains No preservative
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

For reconstitution, add 100 µL distilled water to obtain a final antibody concentration of approximately 1 mg/mL.
For conjugation experiments using this carrier-free antibody, perform an additional desalting step (Zeba Spin Desalting Columns, 7K MWCO, 0.5 mL, Product #89882).

Target Information

Mutations in the GNAS gene are associated with several disorders, including:

  • Pseudohypoparathyroidism types 1a and 1b
  • Albright hereditary osteodystrophy
  • Pseudopseudohypoparathyroidism
  • McCune-Albright syndrome
  • Progressive osseous heteroplasia
  • Polyostotic fibrous dysplasia
  • Certain pituitary tumors

The GNAS gene has a complex imprinted expression pattern, encoding multiple alternatively spliced transcripts with distinct 5′ exons located within differentially methylated regions. Some transcripts show unusual promoter proximity (14 kb apart), and one variant introduces a frameshift resulting in a structurally unrelated isoform. An antisense transcript may regulate imprinting in this region. Mutations lead to pseudohypoparathyroidism type 1a (PHP1a), which exhibits atypical autosomal dominant inheritance requiring maternal transmission for full penetrance.


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

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