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Thermo Fisher Scientific GNAS Monoclonal Antibody (A8F11)
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Thermo Fisher Scientific GNAS Monoclonal Antibody (A8F11)

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GNAS 단백질을 인식하는 Thermo Fisher Scientific의 단클론 항체(A8F11). Western blot, IHC, ICC 등 다양한 응용에 적합하며, 인간, 마우스, 랫트 시료에 반응. Protein A로 정제된 액상 항체로, 장기 보관 시 -20°C에서 안정적 유지 가능.

카탈로그번호
MA544920
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오후 03:48
Thermo Fisher Scientific MA544920 GNAS Monoclonal Antibody (A8F11) 100 ul pk판매 단위 pk ·
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697,000원VAT 포함 766,700원

Thermo Fisher Scientific · Thermo Fisher Scientific GNAS Monoclonal Antibody (A8F11)

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:1,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:2,000
Immunocytochemistry (ICC/IF) 1:100

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Mouse / IgG2b
Class Monoclonal
Type Antibody
Clone A8F11
Immunogen Recombinant protein within human GNAS aa 2–251
Conjugate Unconjugated
Form Liquid
Concentration 2 mg/mL
Purification Protein A
Storage Buffer PBS, pH 7.4, with 40% glycerol, 0.1% 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 Ambient (domestic); Wet ice (international)
RRID AB_2931376

Target Information

Mutations in the GNAS gene are associated with a variety of disorders, including pseudohypoparathyroidism type 1a and 1b, Albright hereditary osteodystrophy, pseudopseudohypoparathyroidism, McCune-Albright syndrome, progressive osseous heteroplasia, polyostotic fibrous dysplasia of bone, and certain pituitary tumors.
The gene exhibits complex imprinted expression, producing maternally, paternally, and biallelically expressed proteins from alternatively spliced transcripts with distinct 5’ exons. Some transcripts introduce frameshifts, resulting in structurally unrelated isoforms. An antisense transcript may also regulate imprinting in this region.
Mutations can lead to pseudohypoparathyroidism type 1a (PHP1a), which follows an atypical autosomal dominant inheritance pattern 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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