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Thermo Fisher Scientific REEP5 Polyclonal Antibody
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Thermo Fisher Scientific REEP5 Polyclonal Antibody

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Rabbit polyclonal antibody targeting human REEP5 protein. Validated for IHC (paraffin) applications. Cross-reactive with human, mouse, rat, and non-human primate. Supplied as liquid, 1 mg/mL in PBS with 0.1% sodium azide. For research use only.

카탈로그번호
PA534152
판매단위
pk
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마지막 업데이트 2025. 08. 02. 오전 08:45
Thermo Fisher Scientific PA534152 REEP5 Polyclonal Antibody 50 ug pk판매 단위 pk ·
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700,900원VAT 포함 770,990원

Thermo Fisher Scientific · Thermo Fisher Scientific REEP5 Polyclonal Antibody

Applications and Tested Dilution

  • Application: Immunohistochemistry (Paraffin) (IHC (P))
  • Tested Dilution: 2.5 µg/mL

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Non-human primate, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic 14 amino acid peptide from N-Terminus of human REEP5
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS
Contains 0.1% sodium azide
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2551505

Product Specific Information

Percent identity with other species by BLAST analysis:
Human, Orangutan, Gibbon, Monkey, Marmoset, Mouse, Rat (100%)
Chicken (93%)
Elephant, Platypus (86%)

Target Information

REEP5 (receptor expression-enhancing protein 5), also known as C5orf18, DP1, TB2, or D5S346, is a 189 amino acid multi-pass membrane protein. It is thought to promote the functional cell surface expression of olfactory receptors.
REEP5 belongs to the DP1 family and is encoded by a gene on chromosome 5, which contains approximately 181 million base pairs and around 1,000 genes (about 6% of human genomic DNA).

Chromosome 5 is associated with several genetic disorders, including:

  • Cockayne syndrome (ERCC8 gene)
  • Familial adenomatous polyposis (APC tumor suppressor gene)
  • Treacher Collins syndrome (TCOF1 gene mutations)
  • Cri du chat syndrome (partial deletion of chromosome 5)
    Deletion of the 5q region or entire chromosome 5 is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.

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

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