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Thermo Fisher Scientific CRX Monoclonal Antibody (4G11)
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Thermo Fisher Scientific CRX Monoclonal Antibody (4G11)

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CRX 단백질을 인식하는 Mouse monoclonal antibody로, Western blot과 ELISA에 적합합니다. 인간 시료에 반응하며, PBS 기반 액상 형태로 제공됩니다. 시냅스 및 광수용체 관련 연구에 유용합니다.

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pk
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마지막 업데이트 2025. 08. 05. 오전 09:52
Thermo Fisher Scientific H00001406-M02 CRX Monoclonal Antibody (4G11) 100 ug pk판매 단위 pk ·
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518,100원VAT 포함 569,910원

Thermo Fisher Scientific · Thermo Fisher Scientific CRX Monoclonal Antibody (4G11)

Applications

Western Blot (WB)

  • Tested Dilution: 1–5 µg/mL

ELISA

  • Tested Dilution: 0.03 ng/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG2a, kappa
Class Monoclonal
Type Antibody
Clone 4G11
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 is as follows:
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.
The CRX gene is also expressed in pinealocytes of the pineal gland and may regulate pineal circadian activity by controlling melatonin synthesis gene expression.
Furthermore, CRX(-) mice exhibit 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 visual pathologies such as CORD, Leber congenital amaurosis (LCA), and retinitis pigmentosa (RP).
All characterized CRX mutations produce disease in heterozygotes; missense mutations affect the homeobox domain, whereas 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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