Merck Millipore代理AB15614-200UL Anti-CNGA3 Antibody;store at -20℃

2025-06-27

货号:AB15614-200UL

品牌:Merck Millipore

规格:1SA

目录价:¥10189.00

市场价格:¥8660.65

会员价格:¥8151.20

金山科研平台,产品价格货期咨询微信:jinshanbio Description: Anti-CNGA3 Antibody | AB15614-200UL View All» Promotional Text: Special Shipping Offer on Antibodies100% Performance Guaranteed View All» Trade Name: Chemicon (Millipore) View All» Specificity: Recognizes CNGA3 (Cyclic nucleotide-gated channel, CNG3). View All» Immunogen: Purified peptide from the C-terminus of rat CNGA3 (Accession number Q9QWN7). View All» Species Reactivity: Rat View All» Species Reactivity Note: The immunogen sequence is 15 of 18 amino acids identical in mouse. View All» Application Notes: Western blot: 1:200 using ECL on rat brain membrane lysate. Immunohistochemistry on frozen rat brain sections. Dilutions should be made using a carrier protein such as BSA (1-3%). Optimal working dilutions must be determined by the end user. View All» Control: Included free of charge with the antibody is 40 μg of control antigen (lyophilized powder). The stock solution of the antigen can be made up using 100 μL of sterile deionized water. For negative control, preincubate 1 μg of peptide with 1 μg of antibody for one hour at room temperature. Optimal concentrations must be determined by the end user. View All» Purification Method: Immunoaffinity purified View All» Presentation: Lyophilized from phosphate buffered saline, pH 7.4, containing 1% BSA, and 0.05% sodium azide as a preservative. Reconstitute with 200 μL of sterile deionized water. Centrifuge antibody preparation before use (10,000 xg for 5 min). View All» Storage Conditions: Maintain lyophilized material at -20°C for up to 12 months after date of receipt. After reconstitution maintain at -20°C in undiluted aliquots for up to 6 months. Avoid repeated freeze/thaw cycles. View All» UniProt Number: Q16281 View All» Entrez Gene Number:

  • NM_001079878.1

  • NM_001298.2

    View All» Gene Symbol:
    • CNGA3

    • CNCG3

    • CCNCalpha

    • CNG3

    • CCNCa

    • ACHM2

    • CCNC1

    • CNG-3

      View All» Alternate Names: Anti-Cyclic nucleotide-gated channel, CNG3 View All» Usage Statement: Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals. View All» Key Applications:
      • Immunohistochemistry

      • Western Blotting

        View All» Entrez Gene Summary: This gene encodes a member of the cyclic nucleotide-gated cation channel protein family which is required for normal vision and olfactory signal transduction. Mutations in this gene are associated with achromatopsia (rod monochromacy) and color blindness. Two alternatively spliced transcripts encoding different isoforms have been described. View All» UniProt Summary: FUNCTION: SwissProt: Q16281 # Visual signal transduction is mediated by a G-protein coupled cascade using cGMP as second messenger. This protein can be activated by cyclic GMP which leads to an opening of the cation channel and thereby causing a depolarization of cone photoreceptors. Induced a flickering channel gating, weakened the outward rectification in the presence of extracellular calcium, increased sensitivity for L-cis diltiazem and enhanced the cAMP efficacy of the channel when coexpressed with CNGB3 (By similarity). Essential for the generation of light-evoked electrical responses in the red-, green- and blue sensitive cones.SIZE: 694 amino acids; 78838 Da SUBUNIT: Heterooligomeric complex with CNGB3.SUBCELLULAR LOCATION: Membrane; Multi-pass membrane protein.TISSUE SPECIFICITY: Prominently expressed in retina.DISEASE: SwissProt: Q16281 # Defects in CNGA3 are a cause of achromatopsia type 2 (ACHM2) [MIM:216900]; also known as total colorblindness or rod monochromacy (RMCH2). ACHM2 is an autosomal recessive condition characterized by day blindness and photophobia. In ACHM2 patients the cones are defective and the subjects see better at night.SIMILARITY: SwissProt: Q16281 ## Belongs to the cyclic nucleotide-gated cation channel (TC 1.A.1.5) family. & Contains 1 cyclic nucleotide-binding domain. View All» Brand Family: Chemicon View All» Product Name: Anti-CNGA3 Antibody | AB15614-200UL View All» Antibody Type: Polyclonal Antibody View All» Qty/Pk: 200 µL View All» Format: Affinity Purified View All» Host: Rabbit View All»

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