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Thermo Fisher Scientific TIS11D Polyclonal Antibody
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Thermo Fisher Scientific TIS11D Polyclonal Antibody

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Rabbit polyclonal antibody specific for Human TIS11D protein. Suitable for IHC applications with dilution range 1:50–1:200. Supplied in liquid form, 0.3 mg/mL concentration. For research use only; not for diagnostic or resale.

카탈로그번호
PA561513
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오전 10:28
Thermo Fisher Scientific PA561513 TIS11D Polyclonal Antibody 100 ul pk판매 단위 pk ·
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847,600원VAT 포함 932,360원

Thermo Fisher Scientific · Thermo Fisher Scientific TIS11D Polyclonal Antibody

Applications

Immunohistochemistry (IHC)

  • Tested Dilution: 1:50–1:200
  • Publications: --

Immunohistochemistry (Paraffin) (IHC (P))

  • Tested Dilution: —
  • Publications: --

Product Specifications

항목 내용
Host/Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human TIS11D. Recombinant protein control fragment (Product # RP-98492)
Conjugate Unconjugated
Form Liquid
Concentration 0.3 mg/mL
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_2648490

Product Specific Information

Immunogen sequence:
MSTTLLSAFY DVDFLCKTEK SLANLNLNNM LDKKAVGTPV AAAPSSGFAP GFLRRHSASN LHALAHPAPS PGSCSPKF

Ortholog sequence identity:

  • Mouse: 94%
  • Rat: 94%

Target Information

TIS11D, also known as ZFP36LA (zinc finger protein 36, C3H type-like 2), BRF2 (butyrate response factor 2), ERF2, or RNF162C, is a 494 amino acid protein that localizes to the nucleus and contains two CSH1-type zinc fingers.
Belonging to the TIS11 family of early response proteins, TIS11D is thought to function as a nuclear transcription factor that binds to 5UUAUUUAUUU-3 core RNA sequences and may regulate growth factor-induced cellular responses.
The gene encoding TIS11D maps to human chromosome 2, which houses over 1,400 genes and comprises nearly 8% of the human genome.
Harlequin ichthyosis, a rare and severe skin deformity, is associated with mutations in the ABCA12 gene, while the lipid metabolic disorder sitosterolemia is associated with defects in the ABCG5 and ABCG8 genes.


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

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