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Thermo Fisher Scientific CORD2 Polyclonal Antibody
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Thermo Fisher Scientific CORD2 Polyclonal Antibody

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Rabbit polyclonal antibody recognizing human, mouse, and rat CORD2 (CRX). Suitable for WB and IHC applications. Lyophilized form, reconstitute in sterile water. Store at 4°C short term or -20°C long term. For research use only.

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마지막 업데이트 2025. 08. 05. 오전 09:55
Thermo Fisher Scientific OSC00278W-100UL CORD2 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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563,100원VAT 포함 619,410원

Thermo Fisher Scientific · Thermo Fisher Scientific CORD2 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution Publications
Western Blot (WB) 1:300–1:2,000 -
Immunohistochemistry (IHC) 1:300–1:2,000 -
Miscellaneous (PubMed) - View 2 publications

Product Specifications

Item Description
Species Reactivity Human, Mouse, Rat
Published Species Not Applicable
Host / Isotype Rabbit / Ig
Class Polyclonal
Type Antibody
Immunogen A synthetic peptide from amino acid region 250–300 of human CORD2 conjugated to an immunogenic carrier protein. Target family: CRX (UniProt ID: O43186-1).
Conjugate Unconjugated
Form Lyophilized
Concentration Not determined
Storage Buffer Whole serum
Contains No preservative
Storage Conditions Store at 4°C short term. For long-term storage, store at -20°C, avoiding freeze/thaw cycles. Glycerol (1:1) may be added for stability.
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

  • Reconstitute in 100 µL of sterile water.
  • Centrifuge to remove any insoluble material.
  • Specificity: CORD2.

Target Information

The cone-rod homeobox-containing gene (CRX) encodes a transcription factor that regulates the expression of multiple photoreceptor genes in the developing retina, including opsin and rhodopsin. CRX binds to the OTX motif (TAATCC/A) upstream of photoreceptor genes and is also expressed in pinealocytes, suggesting a role in circadian regulation via melatonin synthesis genes.
Mutations in CRX are associated with cone-rod dystrophy-2 (CORD2), Leber congenital amaurosis (LCA), and retinitis pigmentosa (RP). These mutations affect transcriptional domains, leading to visual disorders.


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

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