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Thermo Fisher Scientific CRALBP Polyclonal Antibody
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Thermo Fisher Scientific CRALBP Polyclonal Antibody

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Thermo Fisher Scientific의 CRALBP Polyclonal Antibody는 인간 및 마우스 시료에 반응하며, Western blot과 Immunocytochemistry에 적합합니다. 항원 친화 크로마토그래피로 정제된 고품질 항체로 시각 관련 단백질 연구에 유용합니다. 장기 보관 시 -20°C에서 안정적으로 유지됩니다.

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마지막 업데이트 2025. 08. 05. 오전 10:49
Thermo Fisher Scientific PA529759 CRALBP Polyclonal Antibody 100 ul pk판매 단위 pk ·
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678,400원VAT 포함 746,240원

Thermo Fisher Scientific · Thermo Fisher Scientific CRALBP Polyclonal Antibody

Applications

Western Blot (WB)

  • Tested Dilution: 1:500–1:3,000

Immunocytochemistry (ICC/IF)

  • Tested Dilution: 1:100–1:1,000
  • Publications: View 1 publication

Product Specifications

항목 내용
Species Reactivity Human, Mouse
Published Species Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant fragment corresponding to a region within amino acids 74–311 of Human CRALBP
Conjugate Unconjugated
Form Liquid
Concentration 1.41 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7, with 20% glycerol
Contains 0.025% ProClin 300
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_2547233

Product Specific Information

  • Recommended positive controls: HepG2, mouse eye
  • Predicted reactivity: Mouse (91%), Rat (91%), Xenopus laevis (82%), Chicken (86%), Bovine (92%)
  • Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.

Target Information

Cellular retinaldehyde-binding protein (CRALBP) plays an important role in the regeneration of 11-cis-retinal for use in rod visual pigments such as opsin and rhodopsin. Once 11-cis-retinal is photoisomerized in the rod outer segment, it is converted to all-trans-retinal and further modified into all-trans-retinol. All-trans-retinol then diffuses into the retinal pigment epithelium (RPE) to be converted back to 11-cis-retinol and further oxidized into 11-cis-retinal (both by CRALBP).
Genetic mutations involving CRALBP’s lack of function have been linked to visual diseases such as bothnia dystrophy, retinitis punctata albescens, retina pigmentosa, and Newfoundland rod-cone dystrophy.
The presence of CRALBP serves as a marker for RPE and Muller glial cells of the retina.


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

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