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Thermo Fisher Scientific MECP2 Recombinant Superclonal Antibody (2HCLC)
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Thermo Fisher Scientific MECP2 Recombinant Superclonal Antibody (2HCLC)

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Recombinant Superclonal™ 항체로 높은 민감도와 일관성을 제공. Human 및 Mouse 반응성, WB 및 ICC/IF에 사용 가능. Protein A로 정제된 액상 항체로 4°C 단기 보관, -20°C 장기 보관 권장. 연구용으로만 사용.

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pk
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Thermo Fisher Scientific 711065 MECP2 Recombinant Superclonal Antibody (2HCLC) 100 ug pk판매 단위 pk
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Thermo Fisher Scientific · Thermo Fisher Scientific MECP2 Recombinant Superclonal Antibody (2HCLC)

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1–2 µg/mL
Immunocytochemistry (ICC/IF) 2 µg/mL

Product Specifications

항목 내용
Species Reactivity Human, Mouse
Host / Isotype Rabbit / IgG
Expression System Expi293
Class Recombinant Superclonal
Type Antibody
Clone 2HCLC
Immunogen Peptides corresponding to Human MECP2 (aa 17–34, 464–475)
Conjugate Unconjugated
Form Liquid
Concentration 0.5 mg/mL
Purification Protein A
Storage Buffer PBS, pH 7.2
Contains 0.09% 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_2608609

Product Specific Information

This antibody is predicted to react with Monkey, Horse, and Pig.
Recombinant rabbit Superclonal™ antibodies are composed of multiple recombinant monoclonal antibodies, combining the sensitivity of polyclonal antibodies with the specificity and consistency of monoclonal antibodies.
These antibodies recognize multiple epitope sites on the target, providing enhanced detection sensitivity for low-abundance targets.
Each lot is produced with a defined mixture of light and heavy chains, minimizing biological variability.
Note: Formerly called “Recombinant Polyclonal Antibody,” now rebranded as “Recombinant Superclonal™ Antibody.” The physical product and performance remain unchanged.

Target Information

MECP2 is a nuclear protein with a methyl-CpG binding domain, capable of binding specifically to methylated DNA.
It plays a critical role in transcriptional repression and mammalian development.
Unlike other MBD family members, MECP2 is X-linked and subject to X inactivation.
Mutations in the MECP2 gene cause most cases of Rett syndrome, a progressive neurological developmental disorder and a common cause of mental retardation in females.


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

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