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RLBP1 antibody (AA 3-288)

The Rabbit Polyclonal anti-RLBP1 antibody has been validated for WB, ELISA and FACS. It is suitable to detect RLBP1 in samples from Human, Rat and Mouse.
Catalog No. ABIN7601185

Quick Overview for RLBP1 antibody (AA 3-288) (ABIN7601185)

Target

See all RLBP1 Antibodies
RLBP1 (Retinaldehyde Binding Protein 1 (RLBP1))

Reactivity

  • 32
  • 5
  • 5
  • 1
  • 1
  • 1
  • 1
Human, Rat, Mouse

Host

  • 25
  • 10
Rabbit

Clonality

  • 25
  • 10
Polyclonal

Conjugate

  • 26
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
This RLBP1 antibody is un-conjugated

Application

  • 23
  • 14
  • 9
  • 9
  • 9
  • 7
  • 5
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • Binding Specificity

    • 15
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 3-288

    Purpose

    Anti-RLBP1 Antibody Picoband®

    Cross-Reactivity (Details)

    No cross-reactivity with other proteins.

    Characteristics

    Anti-RLBP1 Antibody Picoband® (ABIN7601185). Tested in ELISA, Flow Cytometry, WB applications. This antibody reacts with Human, Mouse, Rat. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.

    Purification

    Immunogen affinity purified.

    Immunogen

    E.coli-derived human RLBP1 recombinant protein (Position: E3-D288).

    Isotype

    IgG
  • Application Notes

    Western blot, 0.25-0.5 μg/mL, Mouse, Rat
    Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
    ELISA, 0.1-0.5 μg/mL, -
    1. Bear, J. C., Nemec, T. F., Kennedy, J. C., Marshall, W. H., Power, A. A., Kolonel, V. M., Burke, G. B. Inbreeding in outport Newfoundland. Am. J. Med. Genet. 29: 649-660, 1988. 2. Burstedt, M. S., Sandgren, O., Holmgren, G., Forsman-Semb, K. Bothnia dystrophy caused by mutations in the cellular retinaldehyde-binding protein gene (RLBP1) on chromosome 15q26. Invest. Ophthal. Vis. Sci. 40: 995-1000, 1999. 3. Burstedt, M. S. I., Forsman-Semb, K., Golovleva, I., Janunger, T., Wachtmeister, L., Sandgren, O. Ocular phenotype of Bothnia dystrophy, an autosomal recessive retinitis pigmentosa associated with an R234W mutation in the RLBP1 gene. Arch Ophthal. 119: 260-267, 2001.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    Concentration

    500 μg/mL

    Buffer

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

    Storage

    4 °C,-20 °C

    Storage Comment

    At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
  • Target

    RLBP1 (Retinaldehyde Binding Protein 1 (RLBP1))

    Alternative Name

    RLBP1

    Background

    Synonyms: POU domain, class 4, transcription factor 1

    Tissue Specificity: Expressed in the brain and the retina. Present in the developing brain, spinal cord and eye.

    Background: Retinaldehyde-binding protein 1 (RLBP1) also known as cellular retinaldehyde-binding protein (CRALBP) is a 36-kD water-soluble protein that in humans is encoded by the RLBP1 gene. The protein encoded by this gene is a 36-kD water-soluble protein which carries 11-cis-retinaldehyde or 11-cis-retinal as physiologic ligands. It may be a functional component of the visual cycle. Mutations of this gene have been associated with severe rod-cone dystrophy, Bothnia dystrophy (nonsyndromic autosomal recessive retinitis pigmentosa) and retinitis punctata albescens.

    Molecular Weight

    36 kDa

    Gene ID

    6017

    UniProt

    P12271
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