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Thermo Fisher Scientific CRX Polyclonal Antibody
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Thermo Fisher Scientific CRX Polyclonal Antibody

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CRX 단백질을 인식하는 Sheep 유래 Polyclonal 항체로, Western blot 및 Immunocytochemistry에 사용 가능. 항원 친화 크로마토그래피로 정제되었으며, 동결건조 형태로 제공. 인간 시료 반응성. 시각 관련 유전자 연구에 적합.

카탈로그번호
PA547897
판매단위
pk
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마지막 업데이트 2025. 08. 01. 오후 05:55
Thermo Fisher Scientific PA547897 CRX Polyclonal Antibody 100 ug pk판매 단위 pk ·
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704,800원VAT 포함 775,280원

Thermo Fisher Scientific · Thermo Fisher Scientific CRX Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution Publications
Western Blot (WB) 1 µg/mL -
Immunocytochemistry (ICC/IF) 5–15 µg/mL 1 publication

Product Specifications

항목 내용
Species Reactivity Human
Published Species Human
Host / Isotype Sheep / IgG
Class Polyclonal
Type Antibody
Immunogen E. coli-derived recombinant human CRX (Ala166–Leu299)
Conjugate Unconjugated
Form Lyophilized
Concentration 0.2 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS with 5% trehalose
Contains No Preservative
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2610298

Product Specific Information

Reconstitute in sterile PBS to a final concentration of 0.2 mg/mL.


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. 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 genes.
CRX-deficient 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 visual pathologies such as CORD, Leber congenital amaurosis (LCA), and retinitis pigmentosa (RP).
All known CRX mutations produce disease in heterozygotes, though no correlation exists between phenotype and mutation type. 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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