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Thermo Fisher Scientific CRX Monoclonal Antibody (2F12)
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Thermo Fisher Scientific CRX Monoclonal Antibody (2F12)

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CRX 단백질을 표적하는 mouse monoclonal antibody (clone 2F12)로, Western blot 및 ELISA에 적합합니다. 인간 및 랫트 시료 반응성이 있으며, PBS buffer에 보존된 액상 형태로 제공됩니다. 시냅스 및 시각 관련 유전자 연구에 유용한 연구용 시약입니다.

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마지막 업데이트 2025. 08. 05. 오후 08:34
Thermo Fisher Scientific H00001406-M03 CRX Monoclonal Antibody (2F12) 100 ug pk판매 단위 pk ·
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518,100원VAT 포함 569,910원

Thermo Fisher Scientific · Thermo Fisher Scientific CRX Monoclonal Antibody (2F12)

Applications

Western Blot (WB)

  • Tested Dilution: 1–5 µg/mL

ELISA

  • Tested Dilution: 0.1 ng/mL

Product Specifications

항목 내용
Species Reactivity Human, Rat
Host / Isotype Mouse / IgG2a, kappa
Class Monoclonal
Type Antibody
Clone 2F12
Immunogen CRX (NP_000545, 1–95 a.a) partial recombinant protein with GST tag (MW of GST tag: 26 kDa)
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:

MMAYMNPGPH YSVNALALSG PSVDLMHQAV PYPSAPRKQR RERTTFTRSQ LEELEALFAK TQYPDVYARE EVALKINLPE SRVQVWFKNR RAKCR

Target Information

The cone-rod homeobox-containing gene (CRX) encodes a transcription factor that coordinates the expression of several photoreceptor genes in the developing retina, including opsin and rhodopsin. Specifically, CRX binds the OTX motif (TAATCC/A) upstream from photoreceptor genes.
CRX is also expressed in pinealocytes of the pineal gland and may regulate circadian activity by controlling melatonin synthesis gene expression.
CRX(-) mice show disruption of circadian rhythms. The human CRX gene maps to chromosome 19q13.3 within the cone-rod dystrophy-2 locus (CORD2).
Mutations in CRX are implicated in CORD, Leber congenital amaurosis (LCA), and retinitis pigmentosa (RP). All characterized CRX mutations cause disease in heterozygotes, though phenotype–mutation correlation is not established. Missense mutations affect the homeobox domain, while frameshift mutations affect the OTX domain.


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

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