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RPGRIP1L Polyclonal antibody, PBS Only

RPGRIP1L Polyclonal Antibody for WB, Indirect ELISA

Cat No. 29778-1-PBS

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse, rat

Applications

WB, Indirect ELISA

Formulation:  PBS Only
Conjugate:  Unconjugated
Size/Concentration: 

-/ -

Freight/Packing: -

Quantity

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Product Information

29778-1-PBS targets RPGRIP1L in WB, Indirect ELISA applications and shows reactivity with human, mouse, rat samples.

Tested Reactivity human, mouse, rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen

CatNo: Ag31168

Product name: Recombinant human RPGRIP1L protein

Source: e coli.-derived, PGEX-4T

Tag: GST

Domain: 1-140 aa of NM_015272

Sequence: MSGPTDETAGDLPVKDTGLNLFGMGGLQETSTTRTMKSRQAVSRVSREELEDRFLRLHDENILLKQHARKQEDKIKRMATKLIRLVNDKKRYERVGGGPKRLGRDVEMEEMIEQLQEKVHELEKQNETLKNRLISAKQQL

Predict reactive species
Full Name RPGRIP1-like
Calculated Molecular Weight 151 kDa
Observed Molecular Weight151 kDa
GenBank Accession NumberNM_015272
Gene Symbol RPGRIP1L
Gene ID (NCBI) 23322
RRIDAB_2923607
Conjugate Unconjugated
FormLiquid
Purification MethodAntigen affinity purification
UNIPROT IDQ68CZ1
Storage Buffer PBS only, pH 7.3.
Storage ConditionsStore at -80°C.

Background Information

RPGRIP1L, also named as FTM, KIAA1005, belongs to the RPGRIP1 family. It negatively regulates signaling through the G-protein coupled thromboxane A2 receptor. RPGRIP1L may be involved in mechanisms like programmed cell death, craniofacial development, patterning of the limbs, and formation of the left-right axis.(PMID:17558409) Defects in RPGRIP1L are the cause of Joubert syndrome type 7 (JBTS7). Defects in RPGRIP1L are the cause of Meckel syndrome type 5 (MKS5).

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