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Recombinant Human MPIG6B protein (rFc Tag)

种属

Human

纯度

>90 %, SDS-PAGE

标签

rFc Tag

生物活性

未测试

Cat no : Eg5762

Print datasheet

Synonyms

C6orf25, G6B, G6B-B, Megakaryocyte and platelet inhibitory receptor G6b, NG31



产品信息

纯度 >90 %, SDS-PAGE
内毒素 <0.1 EU/μg protein, LAL method
生物活性
Not tested
来源 HEK293-derived Human MPIG6B protein Asn18-Gln142 (Accession# O95866-1) with a rabbit IgG Fc tag at the C-terminus.
基因ID 80739
蛋白编号 O95866-1
预测分子量 39.0 kDa
SDS-PAGE 40-50 kDa, reducing (R) conditions
组分 Lyophilized from 0.22 μm filtered solution in PBS, pH 7.4. Normally 5% trehalose and 5% mannitol are added as protectants before lyophilization.
复溶 Briefly centrifuge the tube before opening. Reconstitute at 0.1-0.5 mg/mL in sterile water.
储存条件
It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
  • Until expiry date, -20℃ to -80℃ as lyophilized proteins.
  • 3 months, -20℃ to -80℃ under sterile conditions after reconstitution.
运输条件 The product is shipped at ambient temperature. Upon receipt, store it immediately at the recommended temperature.

背景信息

MPIG6B (megakaryocyte and platelet inhibitory receptor G6b), also known as G6b-B or C6orf25, is a lineage-specific immunoreceptor tyrosine-based inhibition motif (ITIM)-containing receptor belonging to the immunoglobulin superfamily. It is predominantly expressed on megakaryocytes and platelets, where it acts as a critical negative regulator of hematopoietic lineage differentiation, megakaryocyte maturation, and platelet production. G6b-B constitutively associates with the tyrosine phosphatases Shp1 and Shp2 to inhibit signaling from ITAM-containing receptors such as GPVI and CLEC-2, thereby attenuating platelet aggregation and activation. Loss-of-function mutations in MPIG6B in humans cause autosomal recessive congenital macrothrombocytopenia with focal myelofibrosis, characterized by severe thrombocytopenia, anemia, and bleeding diathesis.

参考文献:

1. Mazharian, Alexandra et al. Science signaling vol. 5,248 ra78. 30 Oct. 2012, 2. Hofmann, Inga et al. Blood vol. 132,13 (2018): 1399-1412. 3. Newland, Stephen A et al. Blood vol. 109,11 (2007): 4806-9. 4. Becker, Isabelle C et al. Blood advances vol. 6,10 (2022): 3155-3161.

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