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Thermo Fisher Scientific TNNT1 Polyclonal Antibody, MaxPab
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Thermo Fisher Scientific TNNT1 Polyclonal Antibody, MaxPab

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TNNT1 단백질을 인식하는 Thermo Fisher Scientific의 폴리클로날 항체로, Western blot에 적합합니다. Human 시료 반응성이 있으며, Affinity chromatography로 정제되었습니다. PBS(pH 7.4)에 보존되어 있으며, 연구용으로만 사용 가능합니다.

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마지막 업데이트 2025. 08. 05. 오후 09:21
Thermo Fisher Scientific H00007138-B01P TNNT1 Polyclonal Antibody, MaxPab 50 ug pk판매 단위 pk ·
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518,100원VAT 포함 569,910원

Thermo Fisher Scientific · Thermo Fisher Scientific TNNT1 Polyclonal Antibody, MaxPab

Applications

  • Western Blot (WB): 1:500–1:1,000

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG
Class Polyclonal
Type Antibody
Immunogen TNNT1 (NP_003274, 1 a.a. ~ 251 a.a) full-length human protein
Conjugate Unconjugated
Form Liquid
Concentration See Label
Purification Affinity chromatography
Storage Buffer PBS, pH 7.4
Contains No preservative
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

Sequence of this protein is as follows:
MSDTEEQEYE EEQPEEEAAE EEEEEEERPK PSRPVVPPLI PPKIPEGERV DFDDIHRKRM EKDLLELQTL IDVHFEQRKK EEEELVALKE RIERRRSERA EQQRFRTEKE RERQAKLAEE KMRKEEEEAK KRAEDDAKKK KVLSNMGAHF GGYLVKAEQK RGKRQTGREM KVRILSERKK PLDIDYMGEE QLREKAQELS DWIHQLESEK FDLMAKLKQQ KYEINVLYNR ISHAQKFRKG AGKGRVGGRW K

Target Information

This gene encodes a protein that is a subunit of troponin, a regulatory complex located on the thin filament of the sarcomere. The complex regulates striated muscle contraction in response to intracellular calcium concentration changes. It consists of three subunits:

  • Troponin C: Binds calcium
  • Troponin T: Binds tropomyosin
  • Troponin I: Inhibitory subunit

This protein is the slow skeletal troponin T subunit. Mutations in this gene cause nemaline myopathy type 5 (Amish nemaline myopathy), a neuromuscular disorder characterized by muscle weakness and rod-shaped inclusions in skeletal muscle fibers, typically leading to respiratory failure in infancy. Multiple transcript variants encoding different isoforms have been identified.


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

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